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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62678생성일: 2026년 10월 25일

Ethyl chloroformate → Tert-butyl ethyl (4-(thiophen-2-yl)-1,2-phenylene)dicarbamate

https://huagongshe.com/reaction/62678

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물tert-Butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamateHCID 57717474—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Tert-butyl ethyl (4-(thiophen-2-yl)-1,2-phenylene)dicarbamateHCID 7100730944%

반응 단계

To a solution of tert-butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamate (0.20 g, 0.69 mmol, 1.0 equiv.) in dichloromethane (4 mL) was added ethyl chloroformate (0.08 mL, 0.83 mmol, 1.2 equiv.), TEA (0.19 mL, 1.37 mmol, 2.0 equiv.) and DMAP (8 mg, 0.07 mmol, 0.1 equiv.) at 0° C. The reaction was warmed to room temperature and stirred for 16 h. The reaction was then diluted with dichloromethane and water. The organic layer was separated, washed with water and brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude material was purified on column chromatography (silica gel, 20% EtOAc/hexanes) to give tert-butyl ethyl (4-(thiophen-2-yl)-1,2-phenylene)dicarbamate (0.11 g, 44% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447030B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-9d1e233295fc4eff9d5a1d8a5e5b8cc4
출처 메모uspto-grants-2016_09