SYNTHESIS OF HALOGENATED ALKOXYETHANE
    1.
    发明公开

    公开(公告)号:US20240317661A1

    公开(公告)日:2024-09-26

    申请号:US18571585

    申请日:2022-06-17

    IPC分类号: C07C41/06 C07C41/42

    CPC分类号: C07C41/06 C07C41/42

    摘要: A process for continuous preparation of halogenated alkoxyethane of general formula XClHC—CF2OR, where X is —Cl or —F and OR is C1-4 alkoxy, the process comprising a step of introducing in a plate reactor reaction components comprising (i) a compound of general formula XClC═CF2, (ii) a base, and (iii) a C1-4 alkanol, wherein a) the plate reactor comprises a fluidic module defining one or more fluidic path(s) through which the reaction components flow as a reaction mixture, and b) the halogenated alkoxyethane is formed at least upon the reaction components mixing, with the so formed halogenated alkoxyethane flowing out of the plate reactor in a reactor effluent.

    PURIFICATION PROCESS
    2.
    发明公开

    公开(公告)号:US20240286986A1

    公开(公告)日:2024-08-29

    申请号:US18571528

    申请日:2022-06-17

    IPC分类号: C07C41/42

    CPC分类号: C07C41/42

    摘要: A process for purifying halogenated alkoxyethane of general formula XClHC—CF2OR, where X is —Cl or —F and OR is C1-4 alkoxy, from a reaction mixture derived from a batch synthetic procedure for producing the halogenated alkoxyethane, the process comprising the steps of: (a) adding one of an amine and an acid to the reaction mixture, (b) adding a polar liquid to the mixture obtained in step a) to induce phase separation and formation of a polar phase and a separate organic phase, the organic phase containing the halogenated alkoxyethane, and (c) adding the other of the amine and the acid not used step (a) to the organic phase obtained in step (b) to thereby purify the halogenated alkoxyethane.

    PROCESSES FOR PURIFYING GLYCOL ETHERS
    3.
    发明公开

    公开(公告)号:US20240150272A1

    公开(公告)日:2024-05-09

    申请号:US18548990

    申请日:2021-05-19

    IPC分类号: C07C41/42

    CPC分类号: C07C41/42

    摘要: A processes for purifying glycol ethers, comprises (a) providing a glycol ether to a first vessel, the glycol ether, the glycol ether having the following formula: R1—O— (CHR2CHR3) O)nR4; wherein R1 is an alkyl group having 1 to 9 carbon atoms or a phenyl group; wherein R2 and R3 each individually is hydrogen, a methyl group or an ethyl group, provided that when R3 is a methyl group or an ethyl group, R2 is hydrogen and provided that when R2 is a methyl group or an ethyl group, R3 is hydrogen; wherein R4 is hydrogen, an alkyl group having 1 to 4 carbon atoms, an acetyl group, or a propionyl group; and wherein n is an integer of 1 to 3; (b) filling the first vessel with inert gas; (c) heating the glycol ether in the first vessel to a sub-boiling temperature, wherein the sub-boiling temperature is at least 15° C. less than the normal boiling point of the glycol ether; (d) cooling the vapor from the first vessel in a second vessel to provide a liquid; and (e) contacting the glycol ether with a mixed bed of ion exchange resins comprising cationic exchange resins and anionic ion exchange resins.

    METHOD FOR PRODUCING SEVOFLURANE
    6.
    发明申请

    公开(公告)号:US20180222834A1

    公开(公告)日:2018-08-09

    申请号:US15473940

    申请日:2017-03-30

    IPC分类号: C07C41/42 C07C41/22

    摘要: An object of the present invention is to remove a compound A from “sevoflurane containing fluoromethyl-1,1,3,3,3-pentafluoroisopropenyl ether (compound A)” so as to collect high-purity sevoflurane. The present invention concerns a method for producing sevoflurane containing substantially no compound A, comprising the following steps of: bringing a composition containing hydrogen fluoride (HF) and water at a mass ratio of 1:1 to 1:30 into contact with a 1st organic liquid containing sevoflurane and a compound A, thereby obtaining a 2nd organic liquid containing the compound A in an amount that is lower than that in the 1st organic liquid (step 1a); and distilling the 2nd organic liquid under the presence of a degradation inhibitor, thereby obtaining sevoflurane containing substantially no compound A as a main distillation fraction (step 2).

    Process for the preparation of dimethyl ether

    公开(公告)号:US09611202B2

    公开(公告)日:2017-04-04

    申请号:US14424522

    申请日:2013-08-14

    申请人: Haldor Topsoe A/S

    IPC分类号: C07C41/42 C07C41/09

    摘要: Process for the preparation of dimethyl ether product by catalytic conversion of synthesis gas to dimethyl ether comprising the steps of contacting a stream of synthesis gas comprising carbon dioxide in a dimethyl ether synthesis step in one or more reactors and with one or more catalysts active in the formation of methanol and dehydration of methanol to dimethyl ether and forming a product mixture comprising dimethyl ether, carbon dioxide and unconverted synthesis gas; cooling and separating the product mixture into a first liquid phase comprising dimethyl ether and carbon dioxide being dissolved in the formed dimethyl ether, and into a first gaseous phase comprising unconverted synthesis gas containing carbon monoxide and carbon dioxide; passing the first liquid phase to a scrubbing zone and contacting the phase with a liquid sorbent being effective in absorption of carbon dioxide; and withdrawing a dimethyl ether product being depleted in carbon dioxide from the scrubbing zone.