METHOD FOR PRODUCING ORGANIC COMPOUND

    公开(公告)号:US20210371391A1

    公开(公告)日:2021-12-02

    申请号:US17396088

    申请日:2021-08-06

    摘要: An object of the present disclosure is to provide a method for producing an organic compound, and a composition. The object is achieved by a method for producing a compound represented by formula (1): wherein X represents —O—, an optionally substituted imino group, or —S—, R1 represents a hydrogen atom or a hydrocarbyl group optionally having at least one substituent, and R2 represents a hydrogen atom or a monovalent organic group, or R1 and R2, together with X and one carbon atom respectively adjacent to R1 and R2, may form a heterocyclic ring optionally having at least one substituent, R3 represents a hydrogen atom or a monovalent organic group, and R4 represents —CF2CH3 or —CH2CHF2; the method including step A of reacting a compound represented by formula (2): wherein the alphabetical symbols are as defined above, with vinylidene fluoride under light irradiation.

    Composition and Method for the Release of Protected Peptides from a Resin
    6.
    发明申请
    Composition and Method for the Release of Protected Peptides from a Resin 有权
    用于从树脂释放保护肽的组合物和方法

    公开(公告)号:US20090221791A1

    公开(公告)日:2009-09-03

    申请号:US12298917

    申请日:2007-04-18

    IPC分类号: C07K7/00 C07C31/38 C07C31/40

    CPC分类号: C07K1/122 C07K1/061

    摘要: The present invention provides a composition and a method for cleaving a peptide from a solid support resin. Hydrochloric acid in an organic water miscible solvent is used to cleave the peptide-resin attachment. Optionally, trifluoroethanol or hexafluoroisopropanol may be added to the cleavage composition to improve results. When using the present cleavage composition, an evaporation or other step to remove carboxylic byproducts is not necessary following the cleavage reaction. After the resin is filtered out of the cleavage mixture, the peptide may be immediately precipitated with water.

    摘要翻译: 本发明提供了从固体支持树脂切割肽的组合物和方法。 使用有机水混溶性溶剂中的盐酸切割肽 - 树脂附着物。 任选地,可以向切割组合物中加入三氟乙醇或六氟异丙醇以改善结果。 当使用本发明的切割组合物时,在切割反应之后不需要蒸发或其它除去羧酸副产物的步骤。 将树脂从裂解混合物中过滤出后,可立即用水沉淀该肽。

    Preparation of .beta.-fluoroalcohols
    10.
    发明授权
    Preparation of .beta.-fluoroalcohols 失效
    制备β-氟醇

    公开(公告)号:US5276218A

    公开(公告)日:1994-01-04

    申请号:US730368

    申请日:1991-07-15

    摘要: Process for the preparation of .beta.-fluoroalcohols of the formula (I) ##STR1## in which R.sup.1 and R.sup.2 represent straight-chain or branched alkyl andR.sup.3 and R.sup.4 represent hydrogen or alkyl,in which epoxides of the formula (II) ##STR2## are reacted with sodium hydrogen fluoride or potassium hydrogen fluoride under pressure in the presence of diluents.

    摘要翻译: 用于制备式(I)的化合物(I)的方法,其中R 1和R 2表示直链或支链烷基,且R 3和R 4表示氢或烷基,其中式(II)的环氧化物 在稀释剂存在下,在压力下使图像(II)与氟化氢钠或氟化氢钾反应。