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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207538Generated: November 2, 2026

Dimethylcarbamoyl Chloride → HCID 66718549, compound

https://huagongshe.com/reaction/2207538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantSodium CarbonateHCID 10340—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHCID 66718399HCID 66718399—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66718549HCID 66718549—

Reaction Conditions

Temperature40 °C

Reaction Steps

(S)-2-(Tetrahydrofuran-3-yloxymethyl)pyridine-1-oxide (24.08 g, 0.123 mol, 1 eq) was dissolved in anhydrous DCM (400 mL). N,N-Dimethylcarbamyl chloride (19.89 g, 0.185 mol, 1.5 eq) was added followed by trimethylsilyl cyanide (18.35 g, 0.185 mol, 1.5 eq). The solution was stirred at 40° C. for 24 hours (solution had turned red). The reaction was cooled to room temperature, then 2 M aqueous Na2CO3 solution was added (80 mL) and stirred overnight. The emulsion was filtered off, leaving the white precipitate behind. The layers were separated and the organic layer was evaporated to leave a brown oil. This was dissolved in ethyl acetate (160 mL), 2-M aqueous Na2CO3 solution (160 mL) was added and stirred for 2 hours. The layers were separated and the organic layer was washed with saturated brine (30 mL), dried over Na2SO4 and evaporated to a brown oil; LC-MS Retention time 1.82 min; (M+H)+ 205.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376443B2
Source datasetuspto-grants-2016_06
ORD IDord-3f4b1b8649b847dda0c52d673c666926
Source noteuspto-grants-2016_06