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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25027Generated: October 25, 2026

Chlorotrimethylsilane → N-(2,6-Dimethylbenzyl)phthalimide

https://huagongshe.com/reaction/25027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant(2,6-Dimethylphenyl)methanolHCID 186748—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-(2,6-Dimethylbenzyl)phthalimideHCID 10825581—

Reaction Steps

To a stirred solution of 2,6-Dimethylbenzyl Alcohol (Step A, 6.59 g, 48.4 mmol) in DMSO (20 ml) was added chlorotrimethylsilane (15.75 ml, 145 mmol) at room temperature, and the mixture was stirred for one hr. To this reaction mixture were added ethyl acetate and water, the organic layer was washed with brine, dried over Na2SO4, filtered and concentrated to give an oil. The oily residue was redissolved in DMF (100 ml) and potassium phthalimide (10.76 g, 58.1 mmol) was added. The reaction mixture was stirred for 16 hours at room temperature, ethyl acetate was added, and the organic layer was washed with 3% Na2CO3, 1 N HCl, dried over Na2SO4, filtered and concentrated to give white solid. The purification was done by flash chromatography on silica gel column (chloroform:methanol 95:5) to provide the title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858602B2
Source datasetuspto-grants-2005_02
ORD IDord-b39a908e70c044be99ef9823cba1f34d
Source noteuspto-grants-2005_02