KR870003052A - 3'-브로모디페닐 에테르의 제조방법 - Google Patents

3'-브로모디페닐 에테르의 제조방법 Download PDF

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KR870003052A
KR870003052A KR1019860002244A KR860002244A KR870003052A KR 870003052 A KR870003052 A KR 870003052A KR 1019860002244 A KR1019860002244 A KR 1019860002244A KR 860002244 A KR860002244 A KR 860002244A KR 870003052 A KR870003052 A KR 870003052A
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diacyl peroxide
diphenyl ether
radicals
equivalents
equivalent
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KR1019860002244A
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KR940005912B1 (ko
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클리포드 레인즈 배리
마이클 자팩스 에드워드
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롬 앤드 하스 캄파니
윌리엄 이. 램버트 3세
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/27Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
    • C07C205/35Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C205/36Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/06Preparation of nitro compounds
    • C07C201/12Preparation of nitro compounds by reactions not involving the formation of nitro groups

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

내용 없음

Description

3'-브로모디페닐 에테르의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (10)

  1. 대기압정도의 불활성 기권하 극성 반양자성 용매내에서 광을 조사하거나 또는 조사함이 없이 일반식(Ⅱ)의 디페닐에테르를 일반식(Ⅲ)의 디아실 퍼옥시드 및 분자브롬(Br2)과 함께 65-150℃의 온도에서 반응시킴을 특징으로 하는, 2-클로로-4-트리 플루오로메틸-3'-브로드-4'-니트로디페닐 에테르의 제조방법.
    식중, R1은 알카리금속 또는 알카리토류금속이고,
    R2및 R3는 각각 알리파틱라디칼, 아로카틱라디칼 또는 알킬아로마틱라디칼임.
  2. 제1항에 있어서, 일반식(Ⅱ)의 디페닐에테르 1당량당 1-5당량의 일반식(Ⅲ)의 디아실 퍼옥시드를 반응시킴을 특징으로 하는 제조방법.
    식중, R1은 알카리금속 또는 알카리토류금속이고,
    R2및 R3는 각각 알리파틱라디칼, 아로마틱라디칼 또는 알킬아로마틱라디칼임.
  3. 제2항에 있어서, 상기 디페닐에테르 1당량당 3당량의 디아실 퍼옥시드를 반응시킴을 특징으로 하는 제조방법.
  4. 제2항에 있어서, 디아실 퍼옥시드가 디아로마틱 디아실 퍼옥시드임을 특징으로 하는 제조방법.
  5. 제4항에 있어서, 디아실 퍼옥시드가 디벤조일 퍼옥시드임을 특징으로 하는 제조방법.
  6. 제1항에 있어서, 일반식(Ⅱ)의 디페닐에테르 1당량당 1-5당량의 브롬(Br2)를 반응시킴을 특징으로 하는 제조방법.
    식중, R1은 알칼리금속 또는 알카리토류금속임.
  7. 제6항에 있어서, 상기 디페닐에테르 1당량당 2당량의 브롬(Br2)을 반응시킴을 특징으로 하는 제조방법.
  8. 제1항에 있어서, 반응온도가 75-110℃임을 특징으로 하는 제조방법.
  9. 제1항에 있어서, 조사되는 광의 세기가 25와트 이상임을 특징으로 하는 제조방법.
  10. 제9항에 있어서, 조사되는 광의 세기가 75와트 이상임을 특징으로 하는 제조방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019860002244A 1985-09-16 1986-03-26 3'-브로모디페닐에테르의 제조방법 KR940005912B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US776,350 1985-09-16
US06/776,350 US4588487A (en) 1985-09-16 1985-09-16 Process for the preparation of 3'-halodiphenylethers

Publications (2)

Publication Number Publication Date
KR870003052A true KR870003052A (ko) 1987-04-14
KR940005912B1 KR940005912B1 (ko) 1994-06-24

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ID=25107144

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KR1019860002244A KR940005912B1 (ko) 1985-09-16 1986-03-26 3'-브로모디페닐에테르의 제조방법

Country Status (8)

Country Link
US (1) US4588487A (ko)
EP (1) EP0218314B1 (ko)
JP (1) JPS6267050A (ko)
KR (1) KR940005912B1 (ko)
AT (1) ATE54134T1 (ko)
AU (1) AU587026B2 (ko)
CA (1) CA1260016A (ko)
DE (1) DE3672246D1 (ko)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4594133A (en) * 1985-09-16 1986-06-10 Rohm And Haas Company Process for preparing 3'-halodiphenylethers
JP4774763B2 (ja) * 2004-03-25 2011-09-14 住友化学株式会社 精製酢酸3−メチル−2−ブテニルの製造方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3966453A (en) * 1972-01-27 1976-06-29 Ishihara Sangyo Kaisha Ltd. Herbicidal 2-halo-4-trifluoromethyl-4'-cyanophenyl-ethers
US3950435A (en) * 1972-01-27 1976-04-13 Ishihara Sangyo Kaisha Ltd. Herbicidal diphenyl ethers
US4046798A (en) * 1973-02-12 1977-09-06 Rohm And Haas Company Herbicidal 4-trifluoromethyl-4'nitrodiphenyl ethers
US4093446A (en) * 1972-03-14 1978-06-06 Rohm And Haas Company Herbicidal 4-trifluoromethyl-4-nitrodiphenyl ethers
CA1079303A (en) * 1973-02-12 1980-06-10 Horst O. Bayer Herbicidal 4-trifluoromethyl-4'-nitrodiphenyl ethers
US4485254A (en) * 1978-08-04 1984-11-27 Rohm And Haas Company Process for preparing phenoxybenzoic acids
US4358308A (en) * 1981-10-19 1982-11-09 Rohm And Haas Company Herbicidal 4-perfluoroacetyl-, 4-perfluoromethylthio-, 4-perfluoromethylsulfinyl-, and 4-perfluoromethylsulfonyl-4'-nitrodiphenyl ethers
US4419124A (en) * 1981-10-19 1983-12-06 Rohm And Haas Company Herbicidal 4-trifluoromethyl-3'-nitrogen-substituted-4'-substituted diphenyl ethers
US4594133A (en) * 1985-09-16 1986-06-10 Rohm And Haas Company Process for preparing 3'-halodiphenylethers

Also Published As

Publication number Publication date
KR940005912B1 (ko) 1994-06-24
JPS6267050A (ja) 1987-03-26
ATE54134T1 (de) 1990-07-15
AU587026B2 (en) 1989-08-03
DE3672246D1 (de) 1990-08-02
CA1260016A (en) 1989-09-26
EP0218314B1 (en) 1990-06-27
EP0218314A1 (en) 1987-04-15
AU5651386A (en) 1987-03-19
US4588487A (en) 1986-05-13

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