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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274025Generated: 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/274025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneacetic acid, 3,4-dimethoxy-, methyl esterHCID 85213—
ReactantSodiumHCID 5360545—
Reactant2,3-dihydro-6-methoxy-1H-isoindol-5-olHCID 10241135—
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 54212729—

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 numberUS05387685
Source datasetuspto-grants-1995_02
ORD IDord-278b8b799112408cad48b628991a6464
Source noteuspto-grants-1995_02