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Oxalyl chloride → 4-(4-Methyl-1H-imidazol-1-yl)benzoyl chloride

HRID 1635856
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HRID 1635856 반응식
[CH3:1][C:2]1[N:3]=[CH:4][N:5]([C:7]2[CH:15]=[CH:14][C:10]([C:11](O)=[O:12])=[CH:9][CH:8]=2)[CH:6]=1.C(Cl)(=O)C([Cl:19])=O>ClCCl.CN(C)C=O>[CH3:1][C:2]1[N:3]=[CH:4][N:5]([C:7]2[CH:15]=[CH:14][C:10]([C:11]([Cl:19])=[O:12])=[CH:9][CH:8]=2)[CH:6]=1
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참가 물질

5

반응물 2

HCID 65578Oxalyl chlorideHCID 22605443HCID 22605443, 화합물

생성물 1

HCID 226054344-(4-Methyl-1H-imidazol-1-yl)benzoyl chloride수율 117.3%

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

실험 절차

To a suspension of 4-(4-methylimidazol-1-yl)benzoic acid (0.80 g) in dichloromethane (25 ml) was added oxalyl chloride (0.50 g) and one drop of dimethylformamide. The mixture was stirred at room temperature for 18 hours and the volatile material was removed under reduced pressure to yield 4-(4-methylimidazol-1-yl)benzoyl chloride (1.02 g), which was utilized without further purification.

후처리

  1. customthe volatile material was removed under reduced pressure

출처 및 근거

ORD 기록
ord-68d696495d0145908b0605b4b9fba5f5
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06511974B1

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