돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1435919생성일: 2026년 10월 26일

2-(Trifluoromethyl)phenyl isocyanate → tert-Butyl (2-(trifluoromethyl)phenyl)carbamate

https://huagongshe.com/reaction/1435919

반응식

참여 물질

역할이름HCID투입량
반응물2-(Trifluoromethyl)phenyl isocyanateHCID 16794—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl (2-(trifluoromethyl)phenyl)carbamateHCID 1503388352%

반응 단계

To a solution of 1-isocyanato-2-(trifluoromethyl)benzene (4.0 g, 21.4 mmol) in 50 mL of THF at 0° C. was added potassium tert-butoxide (32.0 mL of a 1M solution in THF, 32 mmol) dropwise. The reaction was allowed to stir for 3 h with warming to ambient temperature and then was quenched with 10 mL of water. The mixture was diluted with ethyl acetate and the organics were washed sequentially with 1N HCl, sat'd. aq. NaHCO3 and brine, dried (MgSO4) and concentrated. The residue was taken up in chloroform, filtered through a pad of silica gel and concentrated to afford 2.9 g (52%) of the title compound which was sufficiently pure to be used without further purification. 1H NMR (CDCl3): δ 8.13 (d, 1H, J=8.2 Hz), 7.56 (d, 1H, J=7.7 Hz), 7.52 (t, 1H, J=8.0 Hz), 7.14 (t, 1H, J=7.7 Hz), 6.80 (broad s, 1H), 1.53 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07618980B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-33e2d8ed26024b4687ddf4f60985f5a7
출처 메모uspto-grants-2009_11