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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1254399생성일: 2026년 10월 25일

4-Nitrophenyl chloroformate → (S)-4-nitrophenyl 2-(t-butoxycarbonylamino)-3-cyclohexylpropylcarbamate

https://huagongshe.com/reaction/1254399

반응식

참여 물질

역할이름HCID투입량
반응물4-Nitrophenyl chloroformateHCID 82129—
반응물Sodium BicarbonateHCID 516892—
반응물(S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamateHCID 10988904—
용매AcetonitrileHCID 6342—
용매TetrahydrofuranHCID 8028—
생성물(S)-4-nitrophenyl 2-(t-butoxycarbonylamino)-3-cyclohexylpropylcarbamateHCID 5938296767%

반응 단계

To a stirred solution of (S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamate (0.65 g, 2.54 mmol) in MeCN (20 mL) and THF (5 mL) was added powdered NaHCO3 (0.43 g, 5.08 mmol) followed by a solution of p-nitrophenyl chloroformate (0.51 g, 5.08 mmol) in MeCN (20 mL) dropwise over 10 min. The mixture was stirred at rt for 2 h, filtered through a pad of Celite and concentrated to leave a white solid. This material was purified by chromatography on a 40-g silica cartridge eluted with a gradient from 0-100% EtOAc in hexanes to afford (S)-tert-butyl 1-(p-nitrophenoxycarbonylamino)-3-cyclohexylpropan-2-ylcarbamate (0.67 g, 67%) as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08455521B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-a7bf90a9f16c4b1f906d4c2dbcf34a8f
출처 메모uspto-grants-2013_06