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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20698Generated: October 25, 2026

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

https://huagongshe.com/reaction/20698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, ((2-bromoethoxy)methyl)-HCID 73833—
ReactantSodium ethoxideHCID 2723922—
ReactantMethyl 3-(2,3-bis(cyclopentyloxy)-4-methoxyphenyl)-3-oxopropanoateHCID 68742690—
SolventEthanolHCID 702—
ProductEthyl 4-(benzyloxy)-2-(2,3-bis(cyclopentyloxy)-4-methoxybenzoyl)butanoateHCID 68741697—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745646B2
Source datasetuspto-grants-2010_06
ORD IDord-b5572fcb9d9044329d31676381ddbca5
Source noteuspto-grants-2010_06