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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780277Generated: November 1, 2026

Dimethylformamide → (4S)-1-t-Butoxycarbonyl-4-phenylthio-N-t-butyl-L-prolinamide

https://huagongshe.com/reaction/1780277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium benzenethiolateHCID 4110039—
Reactant(4R)-1-t-butoxycarbonyl-4-(p-toluenesulfonyloxy)-N-t-butyl-L-prolinamideHCID 86750836—
SolventEthyl AcetateHCID 8857—
Product(4S)-1-t-Butoxycarbonyl-4-phenylthio-N-t-butyl-L-prolinamideHCID 5706049385.8%

Reaction Steps

0.45 g (3.41 mmol) of sodium thiophenolate was added to a solution of 1.23 g (3.08 mmol) of (4R)-1-t-butoxycarbonyl-4-(p-toluenesulfonyloxy)-N-t-butyl-L-prolinamide [prepared as described in Preparation 6(a)] in 10 ml of a 2:1 by volume mixture of dimethylformamide and ethyl acetate, and the mixture was stirred for 3 hours. At the end of this time, the reaction mixture was poured into a 10% w/v aqueous solution of sodium hydrogen-carbonate and extracted with ethyl acetate. The organic extract was dried over anhydrous sodium sulfate, and then the solvent was removed by distillation under reduced pressure. The resulting residue was purified by preparative thin layer chromatography, using a 1:3 by volume mixture of ethyl acetate and hexane as the developing solvent, to give 1.0 g of the title compound as a colorless powder, melting at 119°-121° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629406
Source datasetuspto-grants-1997_05
ORD IDord-4c9650e99d1c4028a70e8bdb0dbb246a
Source noteuspto-grants-1997_05