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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748410Generated: October 30, 2026

Dimethylcarbamoyl Chloride → HCID 22939349, compound

https://huagongshe.com/reaction/748410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactanttert-Butyl 3-(pyridin-4-yl)propanoateHCID 14799559—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 22939349HCID 2293934980%

Reaction Steps

tert-Butyl 3-(4-pyridyl)propionate (0.58 g, 2.8 mmol) was dissolved in ethyl acetate (4 ml), and 3-chloroperbenzoic acid (ca. 77%, 0.65 g, 2.9 mmol) was added thereto. The reaction mixture was stirred at room temperature for 18 hrs and subjected to a silica gel (35 g) column chromatography. The fractions eluted with ethyl acetate-ethanol (3:1, v/v) were collected and concentrated. The residue was dissolved in nitroethane (4 ml), and trimethylsilyl cyanide (0.50 g, 5.1 mmol) and N,N-dimethylcarbamoyl chloride (0.54 g, 5.1 mmol) were added thereto. The reaction mixture was stirred at room temperature for 16 hrs and combined with ethyl acetate and water. The organic layer was successively washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine and dried over anhydrous 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 (4:1, v/v) were collected and concentrated to give the titled compound (0.52 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399759B2
Source datasetuspto-grants-2008_07
ORD IDord-4e1613c2047b4239a96a36c8f168ce73
Source noteuspto-grants-2008_07