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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477953Generated: October 30, 2026

Dimethyl Sulfate → HCID 14666748, compound

https://huagongshe.com/reaction/477953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantSodium HydroxideHCID 14798—
ReactantRo 19-8022HCID 3035058—
CatalystTetrabutylammonium IodideHCID 67553—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 14666748HCID 14666748—

Reaction Steps

432 mg of (R)-1-[(10-chloro-4-oxo-3-phenyl-4H-benzo[a]quinolizin-1-yl)carbonyl]-2-pyrrolidinemethanol and 4 mg of tetrabutylammonium iodide in 2 ml of methylene chloride were held in an ultrasound bath for 30 minutes with 104 mg of sodium hydroxide in 0.1 ml of water. 0.19 ml of dimethyl sulfate was then added. After about 1 hour, an additional 0.19 ml of dimethyl sulfate was added and the mixture was allowed to react for an additional 90 minutes. The mixture was diluted with methylene chloride, washed with water, dried over sodium sulfate, filtered and evaporated. The residue was chromatographed on silica gel and the product was recrystallized from cyclohexane/ethanol. There was obtained (R)-1-[(10-chloro-4-oxo-3-phenyl-4H-benzo[a]quinolizin-1-yl)carbonyl]-2-methoxymethylpyrrolidine as yellow crystals of m.p. 137°-140°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04889848
Source datasetuspto-grants-1989_12
ORD IDord-678ab08fb2f74c1cb7026a76c3da545f
Source noteuspto-grants-1989_12