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HRID 28245作成日:2026年10月25日

Hydrochloric Acid → Phenol, 4-nitro-2-(trifluoromethyl)-

https://huagongshe.com/reaction/28245

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium HydroxideHCID 14797—
反応物2-Chloro-5-nitrobenzotrifluorideHCID 61213—
触媒Tetraethylammonium ChlorideHCID 5946—
溶媒MethanolHCID 887—
生成物Phenol, 4-nitro-2-(trifluoromethyl)-HCID 3014014—

反応条件

温度80 °C

反応手順

450 g of 2-chloro-5-nitro-benzotrifluoride in 1,250 ml of methanol and 35 g of tetraethylammonium chloride are initially introduced. 1,000 g of an aqueous, 50% strength potassium hydroxide solution are then added dropwise (1 hour), the temperature being kept at a maximum of 40° C. by cooling. About 30 minutes after the addition has ended, the mixture is heated to 80° C. for 6 hours, cooled and rendered acid with concentrated hydrochloric acid. The mixture is extracted several times with 300 ml of methylene chloride each time, and the organic phase is dried with sodium sulphate and freed from the solvent under reduced pressure. About 413 g of crude product, melting point: 90°-95° C., are obtained with a purity of about 95% according to analysis by gas chromatography. After recrystallisation from toluene, or distillation under 0.5 mm, pure 4-nitro-2-trifluoromethylphenol is obtained, melting point: 134° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04225731
出典データセットuspto-grants-1980_09
ORD IDord-65f8aedb14bb489f9cd955c8f6bc1dcc
出典メモuspto-grants-1980_09