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HRID 261935作成日:2026年10月27日

4-Chlorobenzophenone → 1-[(Benzyloxy)methyl]-alpha-(p-chlorophenyl)-alpha-phenylimidazole-2-methanol

https://huagongshe.com/reaction/261935

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorobenzophenoneHCID 8653—
反応物1-BenzyloxymethylimidazoleHCID 14795908—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物1-[(Benzyloxy)methyl]-alpha-(p-chlorophenyl)-alpha-phenylimidazole-2-methanolHCID 12433915—

反応手順

To a solution of 11.8 g. of 1-[(benzyloxy)methyl]imidazole in 100 ml. of anhydrous tetrahydrofuran and 50 ml. of anhydrous diethyl ether a solution of 38 ml. of a 20% butyllithium suspension in hexane dissolved in 75 ml. of anhydrous diethyl ether was added drop-wise with stirring at room temperature. Thereafter a solution of 14.6 g. of 4-chlorobenzophenone in 100 ml. of anhydrous tetrahydrofuran and 50 ml. of anhydrous diethyl ether was added drop-wise at room temperature. The mixture was kept for three hours and then extracted with a dilute acid solution. The acidic aqueous layer was made alkaline with 2 N sodium hydroxide solution and extracted with diethyl ether. Part of the ether was removed by evaporation and the residue washed with water. The ether solution was again concentrated and the desired compound crystallised from a mixture of toluene and petroleum ether (boiling range 28°-40° C.). Melting point of the product was 114.5°-117° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04152441
出典データセットuspto-grants-1979_05
ORD IDord-39d68689ec82426b914e67b3c5e74115
出典メモuspto-grants-1979_05