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3-Chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid → 3-Chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid anhydride

HRID 1906090
노트
인쇄 미리보기

반응식

HRID 1906090 반응식
[Cl:1][C:2]1[C:6]2=[N:7][C:8]([C:14]([OH:16])=[O:15])=[C:9]([C:11]([OH:13])=O)[CH:10]=[C:5]2[S:4][CH:3]=1>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[C:6]2=[N:7][C:8]3[C:14](=[O:15])[O:16][C:11](=[O:13])[C:9]=3[CH:10]=[C:5]2[S:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 148387283-Chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid

생성물 1

HCID 137524853-Chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid anhydride수율 89%

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

3-Chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid (1.45 g) is heated at 85° to 90° C. for 30 minutes then 90° to 102° C. for 30 minutes in acetic anhydride (7 mL). The reaction is cooled, the solids filtered off and washed with ether to give 1.2 g of 3-chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid anhydride. The proton magnetic resonance spectrum is consistant with the structure.

후처리

  1. temperatureThe reaction is cooled
  2. filtrationthe solids filtered off
  3. washwashed with ether

출처 및 근거

ORD 기록
ord-c104cae14b824a67b426c156a726c791
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04650514

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