KR950032071A - 4-할로-2'-니트로부티로페논 화합물의 제조 방법 - Google Patents

4-할로-2'-니트로부티로페논 화합물의 제조 방법 Download PDF

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KR950032071A
KR950032071A KR1019950009935A KR19950009935A KR950032071A KR 950032071 A KR950032071 A KR 950032071A KR 1019950009935 A KR1019950009935 A KR 1019950009935A KR 19950009935 A KR19950009935 A KR 19950009935A KR 950032071 A KR950032071 A KR 950032071A
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South Korea
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solvent
compound
halo
formula
xylene
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KR1019950009935A
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KR100343658B1 (ko
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앤드류스 코오터즈 데이빗
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알퐁스 아아르 노에
아메리칸 사이아나밋드 캄파니
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/07Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms
    • C07C205/11Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C221/00Preparation of compounds containing amino groups and doubly-bound oxygen atoms bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/02Systems containing only non-condensed rings with a three-membered ring

Abstract

본 발명은 하기 일반 구조식 I
을 갖는 4-할로-2′-니트로부티로페논 화합물의 제조 방법을 제공한다.
일반식 Ⅰ화합물은 설파오일 우레아 제초제의 제조에 있어서 중요한 중간체이다.

Description

4-할로-2′-니트로부티로페논 화합물의 제조 방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (9)

  1. 하기 일반 구조식
    (식에서 X는 C1또는Br 이고; 및 R은 수소, 할로겐, C1-C4알킬 또는 C1-4할로알킬이다)을 갖는 4-할로-2′-니트로부티로페논 화합물을 제조하는 방법으로서, 하기 일반 구조식
    (식에서 X 및 R은 상기 서술된 바와 같다)을 갖는 2-니트로벤조일 할라이드 화합물을 승온의 용매 존재하에 아세틸부티로락톤의 마그네슘 이놀레이트 1당량 이상과 반응시키고 임의로 결과 얻어진 반응 혼합물을 용매를 증류시킴으로써 농축하는 것으로 구성되는 방법.
  2. 제1항에 있어서, 승온이 약 75℃-150℃인 방법.
  3. 제2항에 있어서, 온도가 약 l00℃-130℃인 방법.
  4. 제1항에 있어서, 용매가 방향족 탄화수소 및 염소화된 방향족 탄화수소로 구성된 군으로부터 선택되는 방법.
  5. 4항에 있어서, 용매가 톨루엔, o-크실렌, m-크실렌, p-크실렌, 벤젠 및 클로로벤젠으로 구성된군으로부터 선택되는 방법.
  6. 제5항에 있어서, 용매가 톨루엔인 방법.
  7. 제1항에 있어서, X가 C1 또는 Br이고, R이 수소 또는 할로겐인 방법.
  8. 제7항에 있어서, X가 C1 또는 Br이고, R이 5′-플루오로인 방법.
  9. 제8항에 있어서, X가 C1 이고, R이 수소인 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019950009935A 1994-04-29 1995-04-26 4-할로-2'-니트로부티로페논화합물의제조방법 KR100343658B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US08/235579 1994-04-29
US08/235,579 US5414136A (en) 1994-04-29 1994-04-29 Method for the preparation of 4-halo-2'-nitrobutyrophenone compounds
US08/235,579 1994-04-29

Publications (2)

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KR950032071A true KR950032071A (ko) 1995-12-20
KR100343658B1 KR100343658B1 (ko) 2002-10-31

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KR1019950009935A KR100343658B1 (ko) 1994-04-29 1995-04-26 4-할로-2'-니트로부티로페논화합물의제조방법

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US (1) US5414136A (ko)
EP (1) EP0682007B1 (ko)
JP (1) JP3663229B2 (ko)
KR (1) KR100343658B1 (ko)
CN (1) CN1070170C (ko)
AT (1) ATE171932T1 (ko)
AU (1) AU697345B2 (ko)
DE (1) DE69505183T2 (ko)
DK (1) DK0682007T3 (ko)
ES (1) ES2123175T3 (ko)
HK (1) HK1009962A1 (ko)
LV (1) LV12185B (ko)
MY (1) MY130190A (ko)
SI (1) SI0682007T1 (ko)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5492884A (en) * 1994-04-29 1996-02-20 American Cyanamid Company 1-[2-(cyclopropylcarbonyl)-4-fluorophenyl]sulfamoyl)-3-(4,6-dimethoxy-2-pyrimidinyl) urea and its herbicidal method of use
US5847140A (en) * 1995-06-06 1998-12-08 American Cyanamid Company Intermediates for the manufacture of herbicidal 1-{ 2-(cyclopropylcarbonyl) Phenyl! Sulfamoyl}-3-(4,6-dialkoxy-2-pyrimidinyl) urea compounds
DE19527577A1 (de) * 1995-07-28 1997-01-30 Basf Ag Schlagzähe thermoplastische Formmasse
US6127576A (en) * 1996-12-20 2000-10-03 American Cyanamid Company Aminophenyl ketone derivatives and a method for the preparation thereof
US5856576A (en) * 1997-02-04 1999-01-05 American Cyanamid Company Aryne intermediates and a process for the preparation thereof
DE60136187D1 (de) 2000-08-11 2008-11-27 Japan Tobacco Inc Calciumrezeptor-antagonisten

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI60559C (fi) * 1975-07-17 1982-02-10 Sumitomo Chemical Co Foerfarande foer framstaellning av ny-(tertiaer amino)-orto-aminobutyrofenonfoereningar
US4622065A (en) * 1984-11-01 1986-11-11 Ppg Industries, Inc. Sulfamoyl urea derivatives
US5009699A (en) * 1990-06-22 1991-04-23 American Cyanamid Company 1-{[O-(cyclopropylcarbonyl)phenyl]sulfamoyl}-3-(4,6-dimethoxy-2-pyrimidinyl)urea herbicidal composition and use
US5280007A (en) * 1991-12-18 1994-01-18 American Cyanamid Company Method for safening rice against the phytotoxic effects of a sulfamoyl urea herbicide
ATE141254T1 (de) * 1992-07-06 1996-08-15 American Cyanamid Co O-nitrophenyl cyclopropyl keton, herbizides zwischenprodukt und verfahren zu seiner herstellung

Also Published As

Publication number Publication date
LV12185A (lv) 1998-12-20
LV12185B (en) 1999-02-20
HK1009962A1 (en) 1999-06-11
US5414136A (en) 1995-05-09
CN1113227A (zh) 1995-12-13
AU697345B2 (en) 1998-10-01
DE69505183D1 (de) 1998-11-12
JP3663229B2 (ja) 2005-06-22
ATE171932T1 (de) 1998-10-15
DE69505183T2 (de) 1999-03-25
DK0682007T3 (da) 1999-02-15
KR100343658B1 (ko) 2002-10-31
AU1762695A (en) 1995-11-02
ES2123175T3 (es) 1999-01-01
EP0682007A1 (en) 1995-11-15
CN1070170C (zh) 2001-08-29
EP0682007B1 (en) 1998-10-07
MY130190A (en) 2007-06-29
SI0682007T1 (en) 1999-04-30
JPH07300445A (ja) 1995-11-14

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