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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2201685생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2201685

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 번호US09365498B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-db55e1f2f4cb4fb69d87d452b8104580
출처 메모uspto-grants-2016_06