돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245938생성일: 2026년 10월 26일

Bromotrichloromethane → (R)-methyl 2-(1-(tert-butoxycarbonylamino)ethyl)oxazole-4-carboxylate

https://huagongshe.com/reaction/245938

반응식

참여 물질

역할이름HCID투입량
반응물BromotrichloromethaneHCID 6383—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2-((R)-1-tert-butoxycarbonylamino-ethyl)-4,5-dihydrooxazole-4-carboxylic acid methyl esterHCID 71279821—
용매DichloromethaneHCID 6344—
생성물(R)-methyl 2-(1-(tert-butoxycarbonylamino)ethyl)oxazole-4-carboxylateHCID 6867122148%

반응 단계

In a round-bottomed flask, 2-((R)-1-tert-butoxycarbonylamino-ethyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester (337 mg, 1.18 mmol) was dissolved in dichloromethane (11 ml). The solution was cooled to −16° C. (NaCl/ice bath) and DBU (0.35 ml, 2.32 mmol) was added. After 5 min, bromotrichloromethane (0.13 ml, 1.33 mmol) was added and the reaction mixture was allowed slowly to warm to room temperature and stirred for 4 days. The reaction was quenched with 0.1 M aqueous HCl and extracted with EtOAc (2×). The combined organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated. The residue was chromatographed over silica gel with EtOAc/hexanes (gradient 0-30% EtOAc) to afford 152 mg (48%) of 2-((R)-1-tert-butoxycarbonylamino-ethyl)-oxazole-4-carboxylic acid methyl ester as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658646B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-d1203247537745eb862daa5a76e28614
출처 메모uspto-grants-2014_02