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HRID 1840303作成日:2026年10月27日

Hydrochloric Acid → 3-Phenyl-5-(2-phenylethyl)isoxazole-4-carboxylic acid

https://huagongshe.com/reaction/1840303

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Benzyl BromideHCID 7498—
反応物5-Methyl-3-phenylisoxazole-4-carboxylic acidHCID 14343—
反応物LithiumHCID 3028194—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物3-Phenyl-5-(2-phenylethyl)isoxazole-4-carboxylic acidHCID 2344790684%

反応条件

温度-78 °C

反応手順

To a solution of 1.5 g of 5-methyl-3-phenyl-4-isoxazolecarboxylic acid in 50 mL of anhydrous tetrahydrofuran stirred at −78° C. under N2 atmosphere, 5.9 mL of a 2.5M solution of n-buthyl lithium in n-hexane was added and the solution was stirred at −78° C. for 2 hours. Afterwards, 0.89 mL of benzyl bromide was added at −78° C. and the solution stirred at room temperature for 2 hours. After overnight resting, the solution was poured into water (300 mL), acidified with hydrochloric acid and extracted with ethyl acetate (2×200 mL). The combined organic layers were washed with water, dried (sodium sulphate) and the solvents were evaporated to dryness. The solid residue was washed with petroleum ether to give 1.82 g (84%) of the title compound as an amorphous solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06680319B2
出典データセットuspto-grants-2004_01
ORD IDord-78b2f2ba443a4c5b8c168a26730894c8
出典メモuspto-grants-2004_01