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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743684Generated: October 31, 2026

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

https://huagongshe.com/reaction/1743684

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 chlomatography 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 numberUS07012071B2
Source datasetuspto-grants-2006_03
ORD IDord-84e904ca7db94a3b9f0a8f893a7bdefa
Source noteuspto-grants-2006_03