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HRID 1845890作成日:2026年10月26日

Triethylamine → 3-Azido-1-benzhydrylazetidine

https://huagongshe.com/reaction/1845890

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Sodium AzideHCID 33557—
反応物1-(Diphenylmethyl)azetidin-3-olHCID 330448—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
生成物3-Azido-1-benzhydrylazetidineHCID 15512652—

反応条件

温度-10 °C

反応手順

1-(diphenylmethyl)-3-hydroxyazetidine (5.5 g, 22.98 mmol) was dissolved in acetonitrile (16.5 mL), triethylamine (3.48 g, 34.45 mmol) was added. The reaction mixture was cooled to −10° C., methylsulfonyl chloride (3.16 g, 27.59 mmol) was added dropwise slowly. After completion of dropwise addition, the reaction was performed at 0° C. for 1 h, The resultant reaction liquid was poured into water, extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, filtered, the filtrate was rotatedly concentrated to dryness to yield a white solid. The resultant white solid was added to N,N-dimethyl formamide (25 mL), sodium azide (5.38 g, 82.73 mmol) was added. The reaction mixture was warmed to 100° C. and the reaction was performed overnight. The resultant reaction liquid was cooled to room temperature, poured into water, extracted with dichloromethane. The organic phase was washed with water, dried over anhydrous sodium sulfate, filtered; the filtrate was rotatedly concentrated to dryness to yield 1-(diphenylmethyl)-3-azidoazetidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08952002B2
出典データセットuspto-grants-2015_02
ORD IDord-ec625a3dc1df4b6ea7157684c11f7365
出典メモuspto-grants-2015_02