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Thionyl Chloride → 4-(2-oxopyridin-1(2H)-yl)benzoyl chloride

HRID 1271721
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반응식

HRID 1271721 반응식
[O:1]=[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]1[C:8]1[CH:16]=[CH:15][C:11]([C:12](O)=[O:13])=[CH:10][CH:9]=1.O=S(Cl)[Cl:19]>ClCCCl>[O:1]=[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]1[C:8]1[CH:16]=[CH:15][C:11]([C:12]([Cl:19])=[O:13])=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 184531904-(2-oxopyridin-1(2H)-yl)benzoic acid

생성물 1

HCID 222404154-(2-oxopyridin-1(2H)-yl)benzoyl chloride

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

4-(2-oxopyridin-1(2H)-yl)benzoic acid (1 g, 4.6 mmol) was ]mixed with 10 mL of 1,2-dichloroethane. To this suspension was added SOCl2 (6 mL), and the mixture was refluxed for 1.5 h. The mixture was reduced in vacuo. The remaining traces of SOCl2 were removed by adding 1,2-dichloroethane (2×5 mL) and evaporating to dryness to yield 4-(2-oxopyridin-1(2H)-yl)benzoyl chloride as a white solid.

후처리

  1. temperaturethe mixture was refluxed for 1.5 h
  2. customThe remaining traces of SOCl2 were removed
  3. additionby adding 1,2-dichloroethane (2×5 mL)
  4. customevaporating to dryness

출처 및 근거

ORD 기록
ord-9a3b8b62b1204cdc908ca53f8022c1a0
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07205318B2

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