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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493492생성일: 2026년 10월 26일

1-benzyl-1H-indole-3-carboxylic acid → 1-benzylindole-3-carbonyl Chloride

https://huagongshe.com/reaction/493492

반응식

참여 물질

역할이름HCID투입량
반응물1-benzyl-1H-indole-3-carboxylic acidHCID 33671—
반응물Oxalyl chlorideHCID 65578—
용매DichloromethaneHCID 6344—
생성물1-benzylindole-3-carbonyl ChlorideHCID 10492228—

반응 단계

Oxalyl chloride (7.1 mL, 81.4 mmol) was added under nitrogen dropwise over 10 minutes to a suspension of 1-benzyl-1H-indole-3-carboxylic acid (4.10 g, 16.3 mmol) in 200 mL of methylene chloride at room temperature. When the oxalyl chloride was added there was an immediate evolution of gas and within 30 minutes all of the solid had dissolved. After the addition of the oxalyl chloride the reaction was stirred at room temperature for 2 h. The solvent and excess oxalyl chloride were removed under reduced pressure. The residue was taken up in benzene and then concentrated to dryness under reduced pressure to give 1-benzyl-1H-indole-3-carbonyl chloride, which was used in the following reaction without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534894B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-077fa6822c9143789210fa82aad8b7a5
출처 메모uspto-grants-2009_05