MY110487A - Vapor phase chlorination of difluoromethyl methyl ether - Google Patents

Vapor phase chlorination of difluoromethyl methyl ether

Info

Publication number
MY110487A
MY110487A MYPI94000614A MYPI19940614A MY110487A MY 110487 A MY110487 A MY 110487A MY PI94000614 A MYPI94000614 A MY PI94000614A MY PI19940614 A MYPI19940614 A MY PI19940614A MY 110487 A MY110487 A MY 110487A
Authority
MY
Malaysia
Prior art keywords
methyl ether
vapor phase
fluorinated
phase chlorination
difluoromethyl methyl
Prior art date
Application number
MYPI94000614A
Other languages
English (en)
Inventor
J Bulka Robert
J O'neill Gerald
Original Assignee
Hampshire Chemical Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US08/025,009 external-priority patent/US5278342A/en
Application filed by Hampshire Chemical Corp filed Critical Hampshire Chemical Corp
Publication of MY110487A publication Critical patent/MY110487A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
    • C07C41/22—Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of halogens; by substitution of halogen atoms by other halogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00—Ethers; Compounds having groups, groups or groups
    • C07C43/02—Ethers
    • C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
    • C07C43/04—Saturated ethers
    • C07C43/12—Saturated ethers containing halogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
MYPI94000614A 1993-03-15 1994-03-16 Vapor phase chlorination of difluoromethyl methyl ether MY110487A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/025,009 US5278342A (en) 1992-03-25 1993-03-15 Vapor phase chlorination of difluoromethyl methyl ether

Publications (1)

Publication Number Publication Date
MY110487A true MY110487A (en) 1998-08-29

Family

ID=21823552

Family Applications (1)

Application Number Title Priority Date Filing Date
MYPI94000614A MY110487A (en) 1993-03-15 1994-03-16 Vapor phase chlorination of difluoromethyl methyl ether

Country Status (8)

Country Link
JP (1) JPH06298693A (ko)
KR (1) KR100285073B1 (ko)
CN (1) CN1054115C (ko)
AU (1) AU669604B2 (ko)
BR (1) BR9401152A (ko)
CA (1) CA2118828A1 (ko)
MY (1) MY110487A (ko)
TW (1) TW252973B (ko)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6886104B2 (ja) 2016-12-29 2021-06-16 セントラル硝子株式会社 ハロゲン化α−フルオロエーテル類の製造方法
JP6974718B2 (ja) * 2017-01-13 2021-12-01 セントラル硝子株式会社 １，２，２，２−テトラフルオロエチルジフルオロメチルエーテル（デスフルラン）の製造方法
WO2018123649A1 (ja) * 2016-12-29 2018-07-05 セントラル硝子株式会社 １，２，２，２－テトラフルオロエチルジフルオロメチルエーテル（デスフルラン）の製造方法
US10683252B2 (en) 2016-12-29 2020-06-16 Central Glass Company, Limited Production method for 1,2,2,2-tetrafluoroethyl difluoromethyl ether (desflurane)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY110269A (en) * 1990-10-02 1998-03-31 Hampshire Chemical Corp Synthesis of fluorinated dimethyl ethers

Also Published As

Publication number Publication date
CN1054115C (zh) 2000-07-05
KR940021492A (ko) 1994-10-19
KR100285073B1 (ko) 2001-04-02
CN1100711A (zh) 1995-03-29
JPH06298693A (ja) 1994-10-25
TW252973B (ko) 1995-08-01
AU5777894A (en) 1994-09-22
CA2118828A1 (en) 1994-09-16
AU669604B2 (en) 1996-06-13
BR9401152A (pt) 1994-11-01

Similar Documents

Publication Publication Date Title
MY107905A (en) Chemical process
EP0877009A4 (en) 1,1,1,3,3-PENTAFLUOROPROPANE PRODUCTION PROCESS
EP0526908A3 (en) Process for production of 1,1,1-trifluoro-2,2-dichloroethane
AU620502B2 (en) Process for production of 1,2,2,2-tetrafluoroethyl difluoromethyl ether
ES8304908A1 (es) Procedimiento continuo de preparacion en fase gaseosa de triclorotrifluoretano, diclorotetrafluoretano y monocloropentafluoretano, en proporciones controladas.
ATE186527T1 (de) Chlorierung von (difluormethyl)methylether und fluorierung der chlorierten produkte
TW340837B (en) Process for obtaining isophorone
MY110487A (en) Vapor phase chlorination of difluoromethyl methyl ether
MY112143A (en) Chlorination of difluoromethyl methyl ether
JPS5527138A (en) Preparation of 1,2,2,2-tetrafluoroethane
MY110269A (en) Synthesis of fluorinated dimethyl ethers
JPS5559121A (en) 1-halo-3-decyne compound
GR3023837T3 (en) Process for the preparation of 1,1,1,2-tetrafluoroethane
ES478879A1 (es) Procedimiento de obtencion en continuo de cloruro de mono- cloracetilo.
AU5225893A (en) Synthesis of fluoromethyl ether
JPS5236604A (en) Preparation of methylchloride and its purification process
JPS56127324A (en) Preparation of methyl chloride
JPS562923A (en) Preparation of chlorinated toluene derivative
EP0295582A3 (en) Process for the preparation of largely perfluorinated alkyl compounds containing chlorine, bromine or iodine as well as ether oxygen and perfluoroalkyl compounds containing chlorine, bromine or iodine as well as ether oxygen
YU216283A (en) Process for obtaining 1,1-dioxopenicillanol-oxymethyl-6-beta-amino-penicillanates
EP0491323A3 (en) Process for the preparation of cyclopropanenitrile derivatives
GB2014982A (en) Vapor phase chlorination of 1, 1-dichlorethane
JPS51138635A (en) Process for preparation of styrene oxide
JPS5645475A (en) 1-(5'-hexynyl)-3-methyl-7-alkylxanthine and its preparation
JPS56103138A (en) Preparation of alpha,alpha,alpha-trifluoro-o-toluic fluoride