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HRID 493492作成日:2026年10月26日

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

https://huagongshe.com/reaction/493492

反応式

関与物質

役割名称HCID仕込み量
反応物1-benzyl-1H-indole-3-carboxylic acidHCID 33671—
反応物Oxalyl chlorideHCID 65578—
溶媒DichloromethaneHCID 6344—
生成物1-benzylindole-3-carbonyl ChlorideHCID 10492228—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534894B2
出典データセットuspto-grants-2009_05
ORD IDord-077fa6822c9143789210fa82aad8b7a5
出典メモuspto-grants-2009_05