KR880000397A - 2-클로로-5-(트리클로로메틸) 피리딘의 3-위치를 선택적으로 염소화시키는 방법 - Google Patents

2-클로로-5-(트리클로로메틸) 피리딘의 3-위치를 선택적으로 염소화시키는 방법 Download PDF

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KR880000397A
KR880000397A KR1019860004478A KR860004478A KR880000397A KR 880000397 A KR880000397 A KR 880000397A KR 1019860004478 A KR1019860004478 A KR 1019860004478A KR 860004478 A KR860004478 A KR 860004478A KR 880000397 A KR880000397 A KR 880000397A
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South Korea
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pyridine
trichloromethyl
chloro
chlorinated
temperature
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KR1019860004478A
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KR880002230B1 (ko
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험프레이스 파울라엘.
엘. 험프 레이스 파울라
제이.디트쉐 토마스
제이. 디트쉐 토마스
엘.빅스바이 제임스
엘. 빅스바이 제임스
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더 다우 케미칼 캄파니
리차드 고든 워터맨
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Priority to KR1019860004478A priority Critical patent/KR880002230B1/ko
Publication of KR880000397A publication Critical patent/KR880000397A/ko
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/61Halogen atoms or nitro radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32Oxygen atoms
    • C07D209/34Oxygen atoms in position 2

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

내용 없음

Description

2-클로로-5-(트리클로로메틸) 피리딘의 3-위치를 선택적으로 염소화시키는 방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (11)

  1. 액상의 2-클로로-5-(트리클로로메틸) 피리딘을 텅스텐, 몰리브덴 또는 루테늄 촉매의 부재하에 압력 446 내지 6996KPa 및 온도 60℃ 내지 180℃에서 적정량의 CI2와 접촉시킴으로써, 2-3-디클로로-5-(트리클로로메틸) 피리딘이 2,6-디클로로-3-(트리클로로메틸) 피리딘에 대하여 적어도 2.8 : 1의 비로 제조됨을 특징으로 하여 2-클로로-5-(트리클로로메틸) 피리딘의 3-위치를 선택적으로 염소화시키는 방법.
  2. 제 1 항에 있어서, 2-클로로-5-(트리클로로메틸) 피리딘의 몰랑에 대하여 과잉몰량의 CI2를 사용하는 방법.
  3. 제 2 항에 있어서, 압력이 적어도 790KPa이고 온도가 100℃ 이상인 방법.
  4. 제 3 항에 있어서, 압력이 1480KPa이고 온도가 140℃ 내지 160℃인 방법.
  5. 제 4 항에 있어서, 온도가 약 150℃인 방법.
  6. 제 5 항에 있어서, 2,3-디클로로-5-(트리클로로메틸) 피리딘을 반응혼합물로부터 분리하는 단계를 추가로 포함하는 방법.
  7. 제 6 항에 있어서, 배치식 공정으로 수행하는 방법.
  8. 제 6 항에 있어서, 연속식 주기공정으로 수행하는 방법.
  9. 제 2 항에 있어서, 2-클로로-5-(트리클로로메틸) 피리딘이 염소화 β-피콜린 및 염소화 피리딘의 혼합물 중에 한 성분으로 공급되는 방법.
  10. 제 9 항에 있어서, 염소화 β-피콜린과 염소화 피리딘의 혼합물이 β-피콜린의 증기상 염소화로부터 수득되는 반응생성혼합물인 방법.
  11. 제 1 항에 있어서, HCI을 반응혼합물에 연속적으로 첨가하는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019860004478A 1986-06-05 1986-06-05 2-클로로-5-(트리클로로메틸)피리딘의 3-위치를 선택적으로 염소화시키는 방법 KR880002230B1 (ko)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019860004478A KR880002230B1 (ko) 1986-06-05 1986-06-05 2-클로로-5-(트리클로로메틸)피리딘의 3-위치를 선택적으로 염소화시키는 방법

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019860004478A KR880002230B1 (ko) 1986-06-05 1986-06-05 2-클로로-5-(트리클로로메틸)피리딘의 3-위치를 선택적으로 염소화시키는 방법

Publications (2)

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KR880000397A true KR880000397A (ko) 1988-03-25
KR880002230B1 KR880002230B1 (ko) 1988-10-20

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KR1019860004478A KR880002230B1 (ko) 1986-06-05 1986-06-05 2-클로로-5-(트리클로로메틸)피리딘의 3-위치를 선택적으로 염소화시키는 방법

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