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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Anhydride → HCID 13345321, 화합물

HRID 1584886
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인쇄 미리보기

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HRID 1584886 반응식
[CH3:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=O)[C:5]([C:11]([OH:13])=[O:12])=[CH:4][CH:3]=1.C(OC(=O)C)(=O)C>ClCCl>[CH3:1][C:2]1[N:7]=[C:6]2[C:8]([O:13][C:11](=[O:12])[C:5]2=[CH:4][CH:3]=1)=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 5425676-Methyl-2,3-pyridinedicarboxylic acid

생성물 1

HCID 13345321HCID 13345321, 화합물수율 68%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
110 °C

실험 절차

A mixture of 6-methylpyridine-2,3-dicarboxylic acid (19.75 g) and acetic anhydride (51 ml) was stirred and heated in an oil bath (bath temperature 110° C.) for 5 hours. The solvent was removed in vacuo and a 2:1 mixture of dichloromethane and ether was added, giving a dark brown solid. A solution of this solid in dichloromethane was passed through a pad of silica gel, eluting with dichloromethane, and the solvent was then evaporated to give partially purified 6-methylpyridine-2,3-dicarboxylic acid anhydride (12.1 g).

후처리

  1. customThe solvent was removed in vacuo
  2. additiona 2:1 mixture of dichloromethane and ether
  3. additionwas added
  4. customgiving a dark brown solid
  5. washeluting with dichloromethane
  6. customthe solvent was then evaporated

출처 및 근거

ORD 기록
ord-1f001ef2cea64ac6a0ed426e344da9d3
출처 데이터셋
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05935973

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