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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44241생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물TriethylamineHCID 8471—
반응물1-(p-Chlorophenyl)cyclopropanecarboxylic acidHCID 98606—
반응물P,P-Diphenylphosphinic azideHCID 199401—
용매TolueneHCID 1140—
생성물Tert-butyl (1-(4-chlorophenyl)cyclopropyl)carbamateHCID 58458569—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541407B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ae2107d120a34bfc8fc62b7007f33355
출처 메모uspto-grants-2013_09