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HRID 3129作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物WaterHCID 962—
反応物TetrahydrofuranHCID 8028—
反応物tert-butyl N-[3-chloro-5-(trifluoromethyl)phenyl]carbamateHCID 18929880—
反応物HCID 178418306HCID 178418306—
溶媒PentaneHCID 8003—
生成物2-(tert-Butoxycarbonyl)-6-chloro-4-trifluoromethylbenzoic acidHCID 1892994782%

反応条件

温度-75 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733910
出典データセットuspto-grants-1998_03
ORD IDord-1eb43454a5ef481dbf4ca95331913c1b
出典メモuspto-grants-1998_03