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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33402Generated: October 28, 2026

Benzyl Chloride → HCID 86603974, compound

https://huagongshe.com/reaction/33402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 57436057HCID 57436057—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86603974HCID 86603974—

Reaction Steps

tert-butyl [1,1-Dimethyl-3-(2-oxo-2,3-dihydro-benzimidazol-1-yl)-propyl]-carbamate, benzyl chloride and potassium-tert-butoxide are stirred overnight at ambient temperature in dimethylsulphoxide. The alkylation product tert-butyl [3-(3-benzyl-2-oxo-2,3-dihydro-benzimidazol-1-yl)-1,1-dimethyl-propyl]-carbamate obtained from the reaction is then treated with trifluoroacetic acid/dichloromethane in order to cleave the protective group. Mass spectroscopy [M+H]+=310.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429583B2
Source datasetuspto-grants-2008_09
ORD IDord-c2e5c1538b2c4aecaeaa1350161d3890
Source noteuspto-grants-2008_09