Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371407Generated: October 30, 2026

Triethylamine → HCID 56629981, compound

https://huagongshe.com/reaction/2371407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,6-Dimethyl-2-(4-nitrobenzyloxycarbonylthio)pyrimidineHCID 13504316—
ReactantHCID 56633484HCID 56633484—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 56629981HCID 56629981—

Reaction Steps

To a solution of (2S,4R)-2-acetoxymethyl-4-hydroxypyrrolidine (22.66 g) in water (100 ml), a solution of S-p-nitrobenzyloxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine (34.45 g) in tetrahydrofuran (453 ml) was added at room temperature, followed by addition of triethylamine (22.54 ml). The resulting mixture was stirred at the same temperature for 30 minutes and diluted with ethyl acetate. The reaction mixture was washed successively with dilute hydrochloric acid and aqueous sodium chloride solution and dried over magnesium sulfate, followed by removal of the solvent. The residue was purified by silica gel column chromatography to give (2S,4R)-1-p-nitrobenzyloxycarbonyl-2-acetoxymethyl4-hydroxypyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05093328
Source datasetuspto-grants-1992_03
ORD IDord-d07369521ec9443aa5407e0e6718f301
Source noteuspto-grants-1992_03