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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 449480생성일: 2026년 10월 25일

Triethylamine → (S)-tert-butyl 1-cyano-2-(4-isopropoxyphenyl)ethylcarbamate

https://huagongshe.com/reaction/449480

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Trichloroacetic anhydrideHCID 20079—
반응물(S)-tert-butyl 1-amino-3-(4-isopropoxyphenyl)-1-oxopropan-2-ylcarbamateHCID 59496729—
용매DichloromethaneHCID 6344—
생성물(S)-tert-butyl 1-cyano-2-(4-isopropoxyphenyl)ethylcarbamateHCID 5949672580%

반응 조건

온도0 °C

반응 단계

Trichloroacetic acid anhydride (120 mg, 0.39 mmol) was added slowly to a solution of (S)-tert-butyl 1-amino-3-(4-isopropoxyphenyl)-1-oxopropan-2-ylcarbamate (50 mg, 0.2 mmol) in methylene chloride (3 mL) and triethylamine (86 uL, 0.62 mmol) at 0° C. The reaction was stirred for 1 h. at 0° C. The reaction was quenched with saturated NaHCO3 and was extracted with ethyl acetate. The organic phase was washed with water, saturated brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure to give the crude product, which was purified by Flash chromatography on a silica gel column (EtOAc:Hexane, 1:3 to 1:1) to obtain the (S)-tert-butyl 1-cyano-2-(4-isopropoxyphenyl)ethylcarbamate (40 mg, 80%) as clear oil. Analytical LCMS (M+Na)+: m/z=327.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481732B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-ded7723687b84368be83e778da5e538d
출처 메모uspto-grants-2013_07