KR960702424A - 할로겐화된 알콜의 제조방법(preparation of halogenated alcohols) - Google Patents

할로겐화된 알콜의 제조방법(preparation of halogenated alcohols)

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Publication number
KR960702424A
KR960702424A KR1019950705247A KR19950705247A KR960702424A KR 960702424 A KR960702424 A KR 960702424A KR 1019950705247 A KR1019950705247 A KR 1019950705247A KR 19950705247 A KR19950705247 A KR 19950705247A KR 960702424 A KR960702424 A KR 960702424A
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KR
South Korea
Prior art keywords
strong base
formula
alkali metal
metal alkoxide
preparation
Prior art date
Application number
KR1019950705247A
Other languages
English (en)
Other versions
KR100239232B1 (ko
Inventor
마틴 찰스 보우던
마이클 드라이스데일 턴벌
Original Assignee
비자야 쿠마리 말리페디
제네카 리미티드
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
Application filed by 비자야 쿠마리 말리페디, 제네카 리미티드 filed Critical 비자야 쿠마리 말리페디
Publication of KR960702424A publication Critical patent/KR960702424A/ko
Application granted granted Critical
Publication of KR100239232B1 publication Critical patent/KR100239232B1/ko

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/36—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal
    • C07C29/38—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/40—Halogenated unsaturated alcohols
    • C07C33/42—Halogenated unsaturated alcohols acyclic
    • C07C33/423—Halogenated unsaturated alcohols acyclic containing only double bonds as unsaturation

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

본 발명은 감염기 및 비활성 용매의 존재하에 하기 식(Ⅱ)의 화합물을 3-메틸부트-2-엔-1-알과 반응시키는 것으로 구성되는 하기 식(Ⅰ)의 할로겐화된 알콜 제조방법에 관한다.
CF3-CXCl-CH(OH)-CH=C(CH3)2(Ⅰ)
식중, X는 클로로 또는 브로모임.
CF3-CHXC1 (Ⅱ)
이의 생성물은 농약 제조를 위한 유용한 중간물질이다. 5-브로모-5-클로로-4-하이드록시-2-메틸-6,6,6-트리플루오로헥스-2-엔은 신규하다.

Description

할로겐화된 알콜의 제조방법 (PREPARATION OF HALOGENATED ALCOHOLS)
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (8)

  1. 강염기 및 비활성 용매의 존재하에 하기식 CF3CHXC1의 화합물을 3-메틸부트-2-엔-1-알과 반응시키는 것으로 구성되는 하기 식의 할로겐화된 알콜을 제조하는 방법.
    CF3-CXC1-CH(OH)-CH=C(CH3)2
    식중, X는 브로모 또는 클로로임.
  2. 제1항에 있어서, 강염기가 알카리 금속 알콕사이드인 방법.
  3. 제1항에 있어서, 비활성 용매가 극성 어프로틱(aprotic) 용매인 방법.
  4. 제1항에 있어서, -80-0℃범위내의 온도에서 수행되는 방법.
  5. 강염기 및 극성 어프로틱 용매의 존재하에 1,1-디클로로-2,2,2-트리플루오로에탄올 3-메딜부트-2-엔-1-알과 반응시키는 것으로 구성되는 5,5-디클로로-4-하이드록시-2-메틸-6,6,6-트리플루오로헥스-2-엔을 제조하는 방법.
  6. 제5항에 있어서, 강염기가 알카리 금속 알콕사이드인 방법.
  7. 제6항에 있어서, 알카리 금속 알콕사이드가 소듐 또는 포타슘 t-부톡사이드인 방법.
  8. 5-브로모-5-클로로-4-하이드록시-2-메틸-6,6,6-트리플루오로헥스-2-엔.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019950705247A 1993-05-28 1994-05-25 할로겐화된 알콜의 제조방법 KR100239232B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB939311142A GB9311142D0 (en) 1993-05-28 1993-05-28 Preparation and use of halogenated alcohols
GB9311142.5 1993-05-28
PCT/GB1994/001140 WO1994027942A1 (en) 1993-05-28 1994-05-25 Preparation of halogenated alcohols

Publications (2)

Publication Number Publication Date
KR960702424A true KR960702424A (ko) 1996-04-27
KR100239232B1 KR100239232B1 (ko) 2000-01-15

Family

ID=10736344

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019950705247A KR100239232B1 (ko) 1993-05-28 1994-05-25 할로겐화된 알콜의 제조방법

Country Status (29)

Country Link
US (1) US5527972A (ko)
EP (1) EP0700373B1 (ko)
JP (1) JP3583130B2 (ko)
KR (1) KR100239232B1 (ko)
CN (2) CN1100743C (ko)
AT (1) ATE165328T1 (ko)
AU (1) AU696685B2 (ko)
BG (1) BG61971B1 (ko)
BR (1) BR9406658A (ko)
CA (1) CA2162896C (ko)
CZ (1) CZ285678B6 (ko)
DE (1) DE69409800T2 (ko)
DK (1) DK0700373T3 (ko)
ES (1) ES2115235T3 (ko)
FI (1) FI955703A0 (ko)
GB (2) GB9311142D0 (ko)
GR (1) GR3026696T3 (ko)
HU (1) HU214303B (ko)
IL (1) IL109792A (ko)
IN (1) IN186997B (ko)
MY (1) MY111102A (ko)
NO (1) NO304937B1 (ko)
NZ (1) NZ266489A (ko)
PH (1) PH30363A (ko)
PL (1) PL178738B1 (ko)
RO (1) RO114323B1 (ko)
RU (1) RU2129538C1 (ko)
SK (1) SK281313B6 (ko)
WO (1) WO1994027942A1 (ko)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9423746D0 (en) * 1994-11-24 1995-01-11 Zeneca Ltd Preparation of halogenated alcohols
GB9423743D0 (en) * 1994-11-24 1995-01-11 Zeneca Ltd Preparation of cyclopropane esters
IL115833A (en) * 1994-11-25 1998-10-27 Zeneca Ltd Acids 6, 6 - Dihalo - 3, 3 - Dimethyl - 5 - Hydroxy - 7, 7, 7 Triplooroheptanoics and their alkaline esters useful as an intermediate product Insecticides
CN113292398B (zh) * 2021-05-18 2022-04-22 常州新东化工发展有限公司 一种连续制备4-氯-1-丁醇的方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2076804A (en) * 1980-05-30 1981-12-09 Shell Int Research Process for the Preparation of a Trihalohydroxyl Compound
US4532020A (en) * 1983-03-09 1985-07-30 Daikin Kogyo Co., Ltd. Process for preparing a β-(fluoroalkyl or fluoroalkenyl)-β-hydroxyalkyne
JPS6289638A (ja) * 1985-10-16 1987-04-24 Sagami Chem Res Center １−置換−２，２−ジハロ−３，３，３−トリフルオロプロパノ−ルおよびその誘導体の製造方法
JPH0742251B2 (ja) * 1985-11-18 1995-05-10 財団法人相模中央化学研究所 １，１，１―トリフルオロ―２，２―ジハロ―５―メチル―４―ヘキセン―３―オール誘導体

Also Published As

Publication number Publication date
CA2162896A1 (en) 1994-12-08
SK149595A3 (en) 1996-04-03
MY111102A (en) 1999-08-30
NO954814L (no) 1995-11-27
GB2278352A (en) 1994-11-30
GR3026696T3 (en) 1998-07-31
BG100159A (bg) 1996-05-31
WO1994027942A1 (en) 1994-12-08
NO954814D0 (no) 1995-11-27
CN1174950C (zh) 2004-11-10
DE69409800D1 (de) 1998-05-28
ES2115235T3 (es) 1998-06-16
IL109792A0 (en) 1994-08-26
AU6800794A (en) 1994-12-20
NO304937B1 (no) 1999-03-08
GB9311142D0 (en) 1993-07-14
BG61971B1 (bg) 1998-11-30
AU696685B2 (en) 1998-09-17
PL311747A1 (en) 1996-03-18
IL109792A (en) 1999-12-31
BR9406658A (pt) 1996-01-30
DE69409800T2 (de) 1998-08-13
ATE165328T1 (de) 1998-05-15
PL178738B1 (pl) 2000-06-30
KR100239232B1 (ko) 2000-01-15
CN1124952A (zh) 1996-06-19
CN1100743C (zh) 2003-02-05
IN186997B (ko) 2001-12-22
JPH09505026A (ja) 1997-05-20
JP3583130B2 (ja) 2004-10-27
DK0700373T3 (da) 1999-02-15
GB2278352B (en) 1996-07-17
EP0700373B1 (en) 1998-04-22
CN1322703A (zh) 2001-11-21
HU214303B (hu) 1998-03-02
CA2162896C (en) 2005-05-03
HU9501636D0 (en) 1996-05-28
GB9410365D0 (en) 1994-07-13
RU2129538C1 (ru) 1999-04-27
HUT74297A (en) 1996-11-28
RO114323B1 (ro) 1999-03-30
NZ266489A (en) 1997-07-27
US5527972A (en) 1996-06-18
FI955703A (fi) 1995-11-27
FI955703A0 (fi) 1995-11-27
PH30363A (en) 1997-04-02
SK281313B6 (sk) 2001-02-12
CZ310895A3 (en) 1996-03-13
CZ285678B6 (cs) 1999-10-13
EP0700373A1 (en) 1996-03-13

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