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HRID 20519作成日:2026年10月24日

Triethylamine → 1-(3,4-Difluorobenzoyl)azetidine

https://huagongshe.com/ja/reaction/20519

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物3,4-Difluorobenzoic acidHCID 99166—
反応物Azetidine hydrochlorideHCID 12308726—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物1-(3,4-Difluorobenzoyl)azetidineHCID 5934685950.7%

反応手順

Oxalyl chloride (1.05 mL, 12.0 mmol) was added to a solution of 3,4-difluorobenzoic acid (1.58 g, 10 mmol) in DCM (50 mL) containing DMF (1 drop). The reaction was stirred at ambient temperature for 16 h then evaporated to dryness. The residue was redissolved in DCM (25 mL) and azetidine hydrochloride (1.12 g, 12.0 mmol) added followed by triethylamine (4.18 mL, 30.0 mmol). The mixture was stirred at ambient temperature for 2 h then concentrated in vacuo. The residue was partitioned between ethyl acetate and 1N hydrochloric acid, the organic phase washed with a saturated aqueous solution of sodium bicarbonate followed by brine, dried (MgSO4), and concentrated in vacuo. The title compound was crystallized from an ethyl acetate/hexane mixture to give a white crystalline solid (1.0 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745475B2
出典データセットuspto-grants-2010_06
ORD IDord-35f62b13bbf54e95be508ca62a2d14d2
出典メモuspto-grants-2010_06