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HRID 3129생성일: 2026년 10월 24일

Carbon Dioxide → 2-(tert-Butoxycarbonyl)-6-chloro-4-trifluoromethylbenzoic acid

https://huagongshe.com/ko/reaction/3129

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물WaterHCID 962—
반응물TetrahydrofuranHCID 8028—
반응물tert-butyl N-[3-chloro-5-(trifluoromethyl)phenyl]carbamateHCID 18929880—
반응물HCID 178418306HCID 178418306—
용매PentaneHCID 8003—
생성물2-(tert-Butoxycarbonyl)-6-chloro-4-trifluoromethylbenzoic acidHCID 1892994782%

반응 조건

온도-75 °C

반응 단계

To a cold (-100° C.) stirred solution of N-(tert-butoxycarbonyl)-3-chloro-5-trifluoromethylaniline 93.4 g, 11.5 mM) in dry tetrahydrofuran (30 mL) under a nitrogen atmosphere was added dropwise t-butyllithium (14.2 mL of 1.7 M solution, 24.2 mM) in pentane. The temperature of the reaction mixture was maintained at -103° to -98° C. during the addition and for 3.25 hr after the addition was completed. Crushed Dry Ice was then added to the cold reaction mixture which, after being allowed to warm to -75° C., was poured into water. The resulting mixture was extracted with ethyl acetate and the combined extracts were dried (MgSO4), filtered and concentrated to leave (3.2 g, 82%) the title compound as a solid white foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733910
출처 데이터셋uspto-grants-1998_03
ORD IDord-1eb43454a5ef481dbf4ca95331913c1b
출처 메모uspto-grants-1998_03