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Thionyl Chloride → HCID 19976091, 화합물

HRID 1450449
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HRID 1450449 반응식
S(Cl)(Cl)=O.[CH3:5][O:6][C:7]1[CH:15]=[CH:14][C:13]([O:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:12][C:8]=1[CH:9]=[N:10]O>C1C=CC=CC=1>[CH3:5][O:6][C:7]1[CH:15]=[CH:14][C:13]([O:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:12][C:8]=1[C:9]#[N:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 73668580HCID 73668580, 화합물

생성물 1

HCID 19976091HCID 19976091, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

Thionyl chloride (11.9 ml, 163 mmol) was added under a nitrogen atmosphere to a suspension of 2-methoxy-5-phenoxybenzaldehyde oxime (3.96 g, 16.3 mmol) in 75 ml of benzene. There was a slight exotherm and the mixture turned yellow. The reaction was heated to reflux temperature over 1 hour and at reflux temperature for an additional hour. The solvent and excess thionyl chloride were removed under reduced pressure to give 2-methoxy-5-phenoxybenzonitrile as a light tan crystalline solid (3.66 g, 100%), mp 88°-89° C.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
temperature
The reaction was heated
  • temperatureto reflux temperature over 1 hour
  • temperatureat reflux temperature for an additional hour
  • customThe solvent and excess thionyl chloride were removed under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-89467a704e614cfdbb9190fb97fdc08b
    출처 데이터셋
    uspto-grants-1997_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05602151

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