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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Oxalyl chloride → 2,3-Dihydro-6-methoxy-1H-indene-1-carbonyl chloride

HRID 1032262
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HRID 1032262 반응식
[CH3:1][O:2][C:3]1[CH:11]=[C:10]2[C:6]([CH2:7][CH2:8][CH:9]2[C:12]([OH:14])=O)=[CH:5][CH:4]=1.C(Cl)(=O)C([Cl:18])=O>C(Cl)Cl.CN(C=O)C>[CH3:1][O:2][C:3]1[CH:11]=[C:10]2[C:6]([CH2:7][CH2:8][CH:9]2[C:12]([Cl:18])=[O:14])=[CH:5][CH:4]=1
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참가 물질

5

반응물 2

HCID 65578Oxalyl chlorideHCID 30471416-Methoxy-2,3-dihydro-1H-indene-1-carboxylic acid

생성물 1

HCID 148226062,3-Dihydro-6-methoxy-1H-indene-1-carbonyl chloride

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

실험 절차

6-Methoxy-indane-1-carboxylic acid, 6.0 g (31 mmol), a compound of Formula 3, was dissolved in 50 ml of methylene chloride and reacted at ambient temperature with 4.0 ml (46 mmol) of oxalyl chloride in the presence of one drop of DMF. After 2 hours, the reaction mixture was brought to reflux and maintained for 15 minutes. It was then concentrated under vacuum and stirred for about 30 minutes, yielding 6-methoxy-indane-1-carboxylic acid chloride, which was sufficiently pure to be used for the next step.

후처리

  1. temperatureto reflux
  2. temperaturemaintained for 15 minutes
  3. concentrationIt was then concentrated under vacuum

출처 및 근거

ORD 기록
ord-1dd86bb3526441e782fc016bbe0fa7f7
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04957914

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