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公开(公告)号:US09409843B2
公开(公告)日:2016-08-09
申请号:US14783706
申请日:2014-04-02
发明人: Takashi Ootsuka , Takashi Masuda , Akihiro Ishii , Mari Imamura , Shunsuke Mimura , Masato Kimura , Hiroshi Minesaki
IPC分类号: C07C45/26 , C07C33/00 , C07C43/00 , C07C49/167 , C07C49/227 , C07C45/45 , C07C33/42 , C07C43/178
CPC分类号: C07C45/26 , C07C33/426 , C07C43/1786 , C07C45/45 , C07C49/167 , C07C49/227
摘要: A production method of a 1,1,1,5,5,5-hexafluoroacetylacetone hydrate according to the present invention includes: step 1: step 1: obtaining a reaction mixture that contains at least 1,1,1,5,5,5-hexafluoro-3-pentyn-2-one or an equivalent thereof by reaction of a 3,3,3-trifluoropropynyl metal with a trifluoroacetate; and step 2: forming the 1,1,1,5,5,5-hexafluoroacetylacetone hydrate by contact of the reaction mixture obtained in the step 1 with water in the presence of an acid. It is possible to produce 1,1,1,5,5,5-hexafluoroacetylacetone by dehydration of the thus-formed hydrate. Thus, the production method according to the present invention is industrially applicable.
摘要翻译: 根据本发明的1,1,1,5,5,5-六氟乙酰丙酮水合物的制备方法包括:步骤1:步骤1:获得含有至少1,1,1,5,5, 通过3,3,3-三氟丙炔基金属与三氟乙酸盐的反应可以得到5-六氟-3-戊炔-2-酮或其等同物; 和步骤2:通过在步骤1中获得的反应混合物与水在酸的存在下接触形成1,1,1,5,5,5-六氟乙酰丙酮水合物。 可以通过如此形成的水合物的脱水制备1,1,1,5,5,5-六氟乙酰丙酮。 因此,本发明的制造方法在工业上是适用的。
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公开(公告)号:US20160075626A1
公开(公告)日:2016-03-17
申请号:US14783706
申请日:2014-04-02
发明人: Takashi OOTSUKA , Takashi MASUDA , Akihiro ISHII , Mari IMAMURA , Shunsuke MIMURA , Masato KIMURA , Hiroshi MINESAKI
IPC分类号: C07C45/26 , C07C43/178 , C07C33/42
CPC分类号: C07C45/26 , C07C33/426 , C07C43/1786 , C07C45/45 , C07C49/167 , C07C49/227
摘要: A production method of a 1,1,1,5,5,5-hexafluoroacetylacetone hydrate according to the present invention includes: step 1: step 1: obtaining a reaction mixture that contains at least 1,1,1,5,5,5-hexafluoro-3-pentyn-2-one or an equivalent thereof by reaction of a 3,3,3-trifluoropropynyl metal with a trifluoroacetate; and step 2: forming the 1,1,1,5,5,5-hexafluoroacetylacetone hydrate by contact of the reaction mixture obtained in the step 1 with water in the presence of an acid. It is possible to produce 1,1,1,5,5,5-hexafluoroacetylacetone by dehydration of the thus-formed hydrate. Thus, the production method according to the present invention is industrially applicable.
摘要翻译: 根据本发明的1,1,1,5,5,5-六氟乙酰丙酮水合物的制备方法包括:步骤1:步骤1:获得含有至少1,1,1,5,5, 通过3,3,3-三氟丙炔基金属与三氟乙酸盐的反应可以得到5-六氟-3-戊炔-2-酮或其等同物; 和步骤2:通过在步骤1中获得的反应混合物与水在酸的存在下接触形成1,1,1,5,5,5-六氟乙酰丙酮水合物。 可以通过如此形成的水合物的脱水制备1,1,1,5,5,5-六氟乙酰丙酮。 因此,本发明的制造方法在工业上是适用的。
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公开(公告)号:US08933275B2
公开(公告)日:2015-01-13
申请号:US13915099
申请日:2013-06-11
申请人: UOP LLC
IPC分类号: C07C45/26 , C07C41/05 , C07C29/44 , B01J19/10 , C07C45/50 , C07C45/34 , C07B41/02 , C07B41/04 , C07C2/82 , C07C29/04 , C07C5/09
CPC分类号: B01J19/10 , B01F5/0475 , B01F15/063 , B01F2015/061 , B01J4/002 , B01J12/005 , B01J12/007 , B01J19/26 , B01J2204/002 , B01J2219/00006 , C07B41/02 , C07B41/04 , C07C2/78 , C07C2/82 , C07C5/09 , C07C29/04 , C07C29/44 , C07C41/05 , C07C45/26 , C07C45/34 , C07C45/50 , C07C47/02 , C07C47/06 , C07C31/08 , C07C11/24 , C07C11/04
摘要: Methods and systems are provided for converting methane in a feed stream to acetylene. The method includes processing acetylene as an intermediate stream to form a stream having oxygenates. The hydrocarbon stream is introduced into a supersonic reactor and pyrolyzed to convert at least a portion of the methane to acetylene. The reactor effluent stream may be treated to convert acetylene to oxygenates through subsequent reactors.
摘要翻译: 提供了将进料流中的甲烷转化为乙炔的方法和系统。 该方法包括处理乙炔作为中间物流以形成具有含氧化合物的物流。 将烃流引入超音速反应器中并热解以将至少一部分甲烷转化为乙炔。 可以处理反应器流出物流以通过后续反应器将乙炔转化为含氧化合物。
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公开(公告)号:US5986111A
公开(公告)日:1999-11-16
申请号:US822323
申请日:1997-03-21
IPC分类号: C07D309/30 , A61K31/366 , C07C45/29 , C07C45/30 , C07C45/38 , C07C47/21 , C07C49/227 , C07C49/258 , C07C57/66 , C07D309/36 , C07D309/38 , C07F7/08 , C07F7/18 , C07C33/03 , C07C45/26 , C07C67/30 , C07D309/32
CPC分类号: C07F7/1856 , A61K31/366 , C07C45/29 , C07C45/298 , C07C45/30 , C07C47/21 , C07C57/66 , C07D309/36 , C07D309/38 , C07F7/0812
摘要: The present invention provides convergent processes for preparing myxopyronins and corallopyronins, compounds useful as antibacterial therapeutics. The present invention also provides novel compositions of matter which are useful for the preparation of pyronin antibiotics.
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公开(公告)号:US4107066A
公开(公告)日:1978-08-15
申请号:US819959
申请日:1977-07-28
IPC分类号: A61K8/35 , A61Q13/00 , C07C29/42 , C07C45/00 , C07C45/26 , C07C45/63 , C07C45/65 , C07C45/66 , C07C45/67 , C07C49/553 , C07C49/557 , C07C49/567 , C07C49/613 , C07C67/00 , C11B9/00 , C11D3/50
CPC分类号: C11D3/50 , C07C29/42 , C07C403/02 , C07C45/26 , C07C45/63 , C07C45/65 , C07C45/66 , C07C45/67 , C07C49/553 , C07C49/567 , C11B9/0053 , C07C2101/16 , C07C2102/28
摘要: Described are hexahydrotetramethyl acetonaphthones and mixtures of such substituted acetonaphthones having the generic formula: ##STR1## wherein one of the dashed lines is a carbon-carbon double bond and each of the other of the dashed lines is a carbon-carbon single bond, and, specifically, the novel isomer having the structure: ##STR2## and processes for the preparation of such mixtures and said novel isomer, as well as a known single component of said mixtures and compounds, by means of first forming 3-chloromesityl oxide from mesityl oxide and chlorine and then reacting the 3-chloromesityl oxide with myrcene via a Diels-Alder reaction thereby producing a chlorine containing Diels-Alder adduct and then either:(i) dehydrochlorinating the chlorine containing Diels-Alder adduct to form an acetyl conjugated cyclohexadiene and cyclizing the acetyl conjugated cyclohexadiene to produce a mixture of isomers having the generic formula: ##STR3## wherein one of the dashed lines is a carbon-carbon double bond and each of the other of the dashed lines is a carbon-carbon single bond; or (II) CYCLIZING THE CHLORINE CONTAINING Diels-Alder adduct to form an acetyl-chloro octahydronaphthalene and dehydrochlorinating the acetylchloro octahydronaphthalene to form a composition substantially composed of a compound having the structure: ##STR4## The products produced are useful as vetiver ingredients in perfumes and perfumed articles.
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公开(公告)号:US2263378A
公开(公告)日:1941-11-18
申请号:US28585939
申请日:1939-07-22
申请人: DU PONT
发明人: SMITH CARTER ALBERT
IPC分类号: C07C45/26
CPC分类号: C07C45/26
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公开(公告)号:US1967225A
公开(公告)日:1934-07-24
申请号:US63053532
申请日:1932-08-26
申请人: DU PONT
发明人: CONAWAY ROLLIN F
IPC分类号: C07C45/26
CPC分类号: C07C45/26 , C07C49/205
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公开(公告)号:US1907882A
公开(公告)日:1933-05-09
申请号:US30483428
申请日:1928-09-08
发明人: LEO SCHLECHT
IPC分类号: C07C45/26
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公开(公告)号:US12017981B2
公开(公告)日:2024-06-25
申请号:US17635515
申请日:2021-04-28
发明人: Yibo Jiang , Yufan Ying , Zheng Li
摘要: Disclosed is a method for preparing acetaldehyde from acetylene under the catalysis of a ZAPO molecular sieve. The method comprises the steps of pre-heating an acetylene raw material gas and water, subjecting same to continuous hydration in a fluidized bed under the catalysis of the ZAPO molecular sieve to prepare acetaldehyde, and then subjecting same to separation, absorption and rectification to obtain an acetaldehyde product, wherein the catalyst can be continuously regenerated for use. The process of the present application is simple, stable and efficient, solves the problem of the dependence nature of the production of acetaldehyde by means of acetylene hydration on a mercury catalyst, avoids the harm caused by mercury to the human body and the environment, and has higher production and use values.
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10.
公开(公告)号:US20230059377A1
公开(公告)日:2023-02-23
申请号:US17635515
申请日:2021-04-28
发明人: Yibo Jiang , Yufan Ying , Zheng Li
摘要: Disclosed is a method for preparing acetaldehyde from acetylene under the catalysis of a ZAPO molecular sieve. The method comprises the steps of pre-heating an acetylene raw material gas and water, subjecting same to continuous hydration in a fluidized bed under the catalysis of the ZAPO molecular sieve to prepare acetaldehyde, and then subjecting same to separation, absorption and rectification to obtain an acetaldehyde product, wherein the catalyst can be continuously regenerated for use. The process of the present application is simple, stable and efficient, solves the problem of the dependence nature of the production of acetaldehyde by means of acetylene hydration on a mercury catalyst, avoids the harm caused by mercury to the human body and the environment, and has higher production and use values.
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