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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684401Generated: October 27, 2026

Benzeneacetic acid, 3,4-dimethoxy-, methyl ester → alpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl ester

https://huagongshe.com/reaction/1684401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneacetic acid, 3,4-dimethoxy-, methyl esterHCID 85213—
ReactantSodiumHCID 5360545—
Reactant(5-Bromopentyl)(1,1-dimethylethyl)dimethyl silaneHCID 19042078—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Productalpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl esterHCID 54212729111.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution, -78° C. under argon, of 2.38 g of 3,4-dimethoxyphenyl acetic acid methyl ester in 30 ml of tetrahydrofuran is added 12.45 ml of 1.0M sodium hexamethylsidilazide. The solution is stirred at -78° C. for 5 minutes and then warmed to 0° C. for 1 hour. To this solution is added 3.5 g of (5-bromopentyl)(1,1-dimethylethyl)dimethyl silane. The reaction mixture is allowed to warm to room temperature and stirred for 12 hours. The mixture is diluted with diethyl ether and water, the layers are separated and the organic layer is washed with saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by chromatography (silica gel: hexane/ethyl acetate,5/1) to give 2.6 g of the desired product as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639887
Source datasetuspto-grants-1997_06
ORD IDord-927c4c9245f948a6bfcb238795262fab
Source noteuspto-grants-1997_06