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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417243Generated: October 31, 2026

Triethylamine → HCID 20741434, compound

https://huagongshe.com/reaction/2417243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(1'R, 3R)-1-(1'-Phenylethyl)-5-oxo-3-pyrrolidine carboxylic acidHCID 723634—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 20741434HCID 2074143482%

Reaction Steps

Oxalyl chloride (6.54 ml, 0.075 mol) and dimethylformamide (3 drops) were added to ice-cooled dichloromethane solution (200 ml) of 1-[1-(R)-phenylethyl]-5-oxopyrrolidine-3-(R)-carboxylic acid (11.66 g, 0.05 mol), and the mixture was stirred overnight at room temperature. After evaporation of the solvent under a reduced pressure, toluene (100 ml) was added and the solvent was again evaporated under a reduced pressure. Dichloromethane (200 ml) and N,O-methylhydroxylamine hydrochloride (5.47 g, 0.055 mol) were added to the resulting residue and, while ice-cooling and stirring, dichloromethane solution (50 ml) of triethylamine (17.4 ml, 0.125 mol) was added dropwise thereto in 15 minutes. After 30 minutes of stirring under ice-cooling, this was stirred at room temperature for 3 hours. The reaction solution was washed with 10% citric acid aqueous solution (100 ml), water (100 ml) and saturated sodium bicarbonate aqueous solution (100 ml) in that order, and then dried over anhydrous sodium sulfate. The solvent was evaporated under a reduced pressure and the residue was subjected to a silica gel column chromatography. By eluting with a chloroform:methanol of from (50:1) to (20:1), 11.32 g (82%) of the title compound was obtained as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825353B2
Source datasetuspto-grants-2004_11
ORD IDord-4e1e40eb00a740c5b4d14ccbb4a1c203
Source noteuspto-grants-2004_11