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HRID 44241作成日:2026年10月24日

tert-Butanol → Tert-butyl (1-(4-chlorophenyl)cyclopropyl)carbamate

https://huagongshe.com/ja/reaction/44241

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物TriethylamineHCID 8471—
反応物1-(p-Chlorophenyl)cyclopropanecarboxylic acidHCID 98606—
反応物P,P-Diphenylphosphinic azideHCID 199401—
溶媒TolueneHCID 1140—
生成物Tert-butyl (1-(4-chlorophenyl)cyclopropyl)carbamateHCID 58458569—

反応条件

温度80 °C

反応手順

A solution of 1-(4-chlorophenyl)cyclopropanecarboxylic acid (10.5 g, 53.3 mmol) in toluene (70 mL) was treated successively with triethylamine (15 mL, 106.6 mmol), diphenylphosphorylazide (DPPA) (12.7 mL, 58.6 mmol) and tert-butanol (25 mL, 267 mmol). The reaction mixture was stirred at 80° C. for 20 hours. The mixture was partitioned between ethyl acetate (300 mL) and water (100 mL). The phases were separated and the organic phase was washed with water (80 mL) then brine (100 mL). The organic phase was dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by flash chromatography (SiO2, 10% ethyl acetate in hexanes). The tert-butyl (1-(4-chlorophenyl)cyclopropyl)carbamate was obtained as a white solid (14 g). LCMS [M+H]: 268.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541407B2
出典データセットuspto-grants-2013_09
ORD IDord-ae2107d120a34bfc8fc62b7007f33355
出典メモuspto-grants-2013_09