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HRID 36373作成日:2026年10月26日

Potassium Hydroxide → Ethyl 2-benzylacrylate

https://huagongshe.com/reaction/36373

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物Diethyl 2-benzylpropanedioateHCID 69090—
溶媒EthanolHCID 702—
生成物Ethyl 2-benzylacrylateHCID 1108464885.5%

反応手順

A mixture of of KOH (8.5 g) in ethanol (100 mL) was added at room temperature to benzylmalonic acid diethyl ester (40 g) in ethanol (80 mL) and the solution was stirred at room temperature overnight, then concentrated by evaporation. Water (14 mL) was added and then the mixture was acidified in an ice bath with concentrated hydrochloric acid (12.6 mL). The mixture was partitioned between water and ether; the organic phase was separated, dried and the ether was evaporated. The residue was treated with pyridine (26 mL), piperidine (1.22 g) and paraformaldehyde (3.56 g). The mixture was heated in an oil bath (130°) for 90 minutes, then cooled, and water (440 mL) was added. The mixture was extracted 3 times with n-hexane (150 mL). The combined organic phases were washed successively with water, 1N HCl, water, saturated NaHCO3 solution and brine. The organic solution was dried (MgSO4) and evaporated to give the title compound as colorless oil (26 g, 85 % yield). 1H NMR: 300MHz spectrum consistent with proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05414018
出典データセットuspto-grants-1995_05
ORD IDord-0924ded253b34cb1b6e3517fb0eb3cab
出典メモuspto-grants-1995_05