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HRID 653145作成日:2026年10月23日

Benzyl Chloride → 1-Phenyl-3-(phenylmethoxy)-1H-indole-2-carboxylic acid methyl ester

https://huagongshe.com/ja/reaction/653145

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物Sodium hydrideHCID 24758—
反応物Methyl 3-hydroxy-1-phenyl-1H-indole-2-carboxylateHCID 54687160—
溶媒HexamethylphosphoramideHCID 12679—
生成物1-Phenyl-3-(phenylmethoxy)-1H-indole-2-carboxylic acid methyl esterHCID 1388582654%

反応手順

A mixture of 1.2 g (0.025 mole) of 50% sodium hydride/mineral oil suspension in 20 ml of hexamethylphosphoramide under a nitrogen atmosphere was cooled in ice and treated over 15 minutes with a solution of 5.3 g (0.020 mole) of 3-hydroxy-1-phenyl-1H-indole-2-carboxlic acid methyl ester [P. Friedlander and K. Kurz, Chem. Ber., 55, 1597 (1922)] in 25 ml of hexamethylphosphoramide. The mixture was stirred in ice an additional one hour, 2.6 ml (2.9 g, 0.023 mole) of benzyl chloride was added in one portion, the ice bath was removed and stirring was continued for a total of 18 hours. The reaction mixture was added to 200 g of ice/water, stirred for one hour, and the precipitated product was filtered and washed with water. Recrystallization from aqueous methanol yielded 3.8 g (54% yield) of the ester product. An additional recrystallization as above yielded analytically pure ester, mp 117°-119° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04675332
出典データセットuspto-grants-1987_06
ORD IDord-bcc7c97dd21844328ed5cb7d5875aa91
出典メモuspto-grants-1987_06