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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37016Generated: October 25, 2026

Hydrochloric Acid → 3-Mercapto-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine

https://huagongshe.com/reaction/37016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidineHCID 54037145—
SolventMethanolHCID 887—
Product3-Mercapto-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidineHCID 5340089275.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 30 g of 3-acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine in 1000 ml of methanol was cooled to -10° C. A solution of sodium methoxide in methanol (prepared from 1.8 g of sodium) was then added dropwise to the cooled solution, after which the mixture was stirred for 30 minutes, whilst gradually raising the temperature to 0° C. At the end of this time, 65.2 ml of 10% w/v hydrochloric acid were added to the reaction mixture, which was then concentrated to half of its original volume by evaporation in vacuo. A saturated aqueous solution of sodium chloride was added to the concentrate and the mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride and then dried, after which the solvent was distilled off under reduced pressure. The residue was purified by chromatography through a column of silica gel, eluted with a 2:1 by volume mixture of benzene and ethyl acetate, to give 20 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE034960
Source datasetuspto-grants-1995_05
ORD IDord-9e8ee3d588db4c8381cf57e71e0c8cfb
Source noteuspto-grants-1995_05