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Thionyl Chloride → 6,7-dihydroxy-2-oxo-2H-1-benzopyran-3-carbonyl chloride

HRID 358445
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반응식

HRID 358445 반응식
[OH:1][C:2]1[C:3]([OH:16])=[CH:4][C:5]2[O:10][C:9](=[O:11])[C:8]([C:12](O)=[O:13])=[CH:7][C:6]=2[CH:15]=1.S(Cl)([Cl:19])=O>CN(C)C=O>[OH:1][C:2]1[C:3]([OH:16])=[CH:4][C:5]2[O:10][C:9](=[O:11])[C:8]([C:12]([Cl:19])=[O:13])=[CH:7][C:6]=2[CH:15]=1
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 139895536,7-Dihydroxycoumarin-3-carboxylic Acid

생성물 1

HCID 212867876,7-dihydroxy-2-oxo-2H-1-benzopyran-3-carbonyl chloride

시약·촉매·용매 1

HCID 6228Dimethylformamide촉매

실험 절차

A mixture of 6,7-dihydroxy-2-oxo-2H-1-benzopyran-3-carboxylic acid (110 mg), thionyl chloride (5 mL), and dimethylformamide (one drop) was stirred for 2 hours at room temperature. The excess thionyl chloride was distilled off in vacuo. Benzene (20 mL) was added, followed by vacuum distillation and vacuum drying, to yield 6,7-dihydroxy-2-oxo-2H-1-benzopyran-3-carbonyl chloride.

후처리

  1. distillationThe excess thionyl chloride was distilled off in vacuo
  2. additionBenzene (20 mL) was added
  3. distillationfollowed by vacuum distillation and vacuum
  4. customdrying

출처 및 근거

ORD 기록
ord-863a20bb54bf471d93e5e18abcfbc03b
출처 데이터셋
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04468394

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