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HRID 20698作成日:2026年10月25日

Benzene, ((2-bromoethoxy)methyl)- → Ethyl 4-(benzyloxy)-2-(2,3-bis(cyclopentyloxy)-4-methoxybenzoyl)butanoate

https://huagongshe.com/reaction/20698

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, ((2-bromoethoxy)methyl)-HCID 73833—
反応物Sodium ethoxideHCID 2723922—
反応物Methyl 3-(2,3-bis(cyclopentyloxy)-4-methoxyphenyl)-3-oxopropanoateHCID 68742690—
溶媒EthanolHCID 702—
生成物Ethyl 4-(benzyloxy)-2-(2,3-bis(cyclopentyloxy)-4-methoxybenzoyl)butanoateHCID 68741697—

反応手順

Sodium ethoxide (2.0 g, 29 mmol) was added to a solution of methyl 3-(2,3-bis(cyclopentyloxy)-4-methoxyphenyl)-3-oxopropanoate (11 g, 29 mmol) and ethanol (150 mL) at rt. After refluxing for 1 h, ((2-bromoethoxy)methyl)benzene (12.5 g, 57.8 mmol) was added and refluxing was continued overnight. The reaction was allowed to cool to rt, concentrated, diluted with ethyl acetate (300 mL), and then washed with brine (50 mL×2). The organic layer was dried, filtered, concentrated, and purified by silica gel chromatography (ethyl acetate:petroleum ether) to give ethyl 4-(benzyloxy)-2-(2,3-bis(cyclopentyloxy)-4-methoxybenzoyl)butanoate: MS (ESI): 525.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745646B2
出典データセットuspto-grants-2010_06
ORD IDord-b5572fcb9d9044329d31676381ddbca5
出典メモuspto-grants-2010_06