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HRID 1461757作成日:2026年10月25日

Ammonium Chloride → 3-[2-(4,5-Diphenyl-2-thiazolyl)ethyl]phenol

https://huagongshe.com/reaction/1461757

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2-Methyl-4,5-diphenylthiazoleHCID 77365—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物[3-(Bromomethyl)phenoxy](tert-butyl)dimethylsilaneHCID 10040514—
反応物ButyllithiumHCID 178418339—
溶媒Hydrochloric AcidHCID 313—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物3-[2-(4,5-Diphenyl-2-thiazolyl)ethyl]phenolHCID 1500690458%

反応条件

温度-78 °C

反応手順

n-Butyllithium (1.53 g, 24 mmol) in hexane (9.5 mL) was added dropwise to a stirred solution of 2-methyl-4,5-diphenylthiazole (5 g, 20 mmol) in dry THF (150mL,) maintained at -78° C. under an atmosphere of nitrogen. After 25 minutes a solution of [3-(bromomethyl)phenoxy]dimethyl(1,1-dimethylethyl)silane (6.60 g, 22mmol) in THF (10mL) was added dropwise, the mixture stirred at -78° C. for 10 minutes and the allowed to warm to room temperature. The reaction mixture was poured onto saturated ammonium chloride solution, extracted with CH2Cl2, the extracts combined, dried over sodium sulfate and concentrated in vacuo to leave an oil which was dissolved in THF (25 mL). A solution of tetra-n-butylammonium fluoride (6.77 g, 26 mmol) in THF (25.86 mL) was added and the mixture stirred at room temperature for 30 minutes before being diluted with 1N HCl solution (100 mL). The mixture was extracted with CH2Cl2, the combined extracts dried over sodium sulfate and concentrated to leave an oil. Chromatography on a column of silica gel using a mixture of hexanes and diethyl ether (2:1) as eluent furnished 3-[2-(4,5-diphenyl-2-thiazolyl)ethyl]phenol (4.13 g, 58%), mp 166°-168° C. after recrystallization from a mixture of hexanes and CH2Cl2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05077305
出典データセットuspto-grants-1991_12
ORD IDord-7919114cf47c4a468378cc435560f90a
出典メモuspto-grants-1991_12