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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499639Generated: November 1, 2026

Dimethylcarbamoyl Chloride → HCID 22939565, compound

https://huagongshe.com/reaction/499639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHCID 22939617HCID 22939617—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 22939565HCID 2293956591%

Reaction Steps

2-(Trimethylsilyl)ethyl 2,2-dimethyl-3-(4-pyridyl)propionate (0.77 g, 2.8 mmol) was dissolved in ethyl acetate (4 ml), and 3-chloroperbenzoic acid (ca. 77%, 0.68 g, 3.0 mmol) was added thereto. The reaction mixture was stirred at room temperature for 5 hrs and subjected to a silica gel (35 g) column chromatography. The fractions eluted with ethyl acetate-ethanol (4:1, v/v) were collected and concentrated. The residue was dissolved in acetonitrile (6 ml), and trimethylsilyl cyanide (0.49 g, 4.9 mmol) and N,N-dimethylcarbamoyl chloride (0.45 g, 4.2 mmol) were added thereto. The reaction mixture was stirred at room temperature for 14 hrs and combined with ethyl acetate and water. The organic layer was successively washed with saturated aqueous sodium hydrogen carbonate solution, 1 N hydrochloric acid and saturated brine and dried over magnesium sulfate. The solvent was evaporated, and the residue was subjected to a silica gel (30 g) column chromatography. The fractions eluted with hexane-ethyl acetate (5:1, v/v) were collected and concentrated to give the titled compound (0.69 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767665B2
Source datasetuspto-grants-2010_08
ORD IDord-76d57d7c2a2d4f7aae41fa79b384b3ed
Source noteuspto-grants-2010_08