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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221051Generated: October 27, 2026

Dimethyl Sulfoxide → (S)-2,2-Diphenyl-2-(pyrrolidin-3-yl)acetamide

https://huagongshe.com/reaction/2221051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-3-(1-carbamoyl-1,1-diphenylmethyl)-1-(7-hydroxyhept-1-yl)pyrrolidineHCID 67428481—
SolventDichloromethaneHCID 6344—
Product(S)-2,2-Diphenyl-2-(pyrrolidin-3-yl)acetamideHCID 13633758149.9%

Reaction Steps

To a stirred solution of (S)-3-(1-carbamoyl-1,1-diphenylmethyl)-1-(7-hydroxyhept-1-yl)pyrrolidine (31.00 g, 78.57 mmol); N,N-diisopropylethylamine (68.4 mL, 392.8 mmol); and methyl sulfoxide (60.7 mL, 785.7 mmol) in dichloromethane (780 mL) under an atmosphere of nitrogen at −15° C., was added sulfur trioxide pyridine complex (37.5 g, 235.71 mmol) portion-wise over a 40 min. period. The reaction mixture was maintained between −10° C. and −20° C. during the addition. The reaction was then stirred in this temperature range for 40±10 min. Deionized water (300 mL) was added and the mixture was stirred for 10 minutes. The organic layer was separated and washed with deionized water (200 mL), followed by saturated aqueous sodium chloride (200 mL) and the organic layer was then dried with magnesium sulfate (10 g). The magnesium sulfate was filtered off and washed with dichloromethane (50 mL) and the solvent was reduced in vacuo. The resultant syrup was washed with petroleum ether (2×200 mL) to remove the remaining pyridine and DMSO and the resulting white solid was dried in vacuo to give 33.02 g of the title intermediate (98% yield; >93% purity by chiral HPLC Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368463B2
Source datasetuspto-grants-2008_05
ORD IDord-4bd2ab42984147318d9528bcc516c788
Source noteuspto-grants-2008_05