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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088283Generated: November 1, 2026

(2R,4S)-1-p-Nitrobenzyloxycarbonyl-2-(4-t-butyloxycarbonylbutyl)-4-acetylthiopyrrolidine → (2R,4S)-1-p-nitrobenzyloxycarbonyl-2-(4-carboxybutyl)-4-acetylthiopyrrolidine

https://huagongshe.com/reaction/1088283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R,4S)-1-p-Nitrobenzyloxycarbonyl-2-(4-t-butyloxycarbonylbutyl)-4-acetylthiopyrrolidineHCID 15671523—
SolventTrifluoroacetic acidHCID 6422—
Product(2R,4S)-1-p-nitrobenzyloxycarbonyl-2-(4-carboxybutyl)-4-acetylthiopyrrolidineHCID 15671524—

Reaction Steps

(2R,4S)-1-p-Nitrobenzyloxycarbonyl-2-(4-t-butyloxycarbonylbutyl)-4-acetylthiopyrrolidine (493 mg) was dissolved in 2.5 ml of trifluoroacetic acid, followed by stirring at room temperature for 15 minutes. The reaction mixture was distilled off to obtain (2R,4S)-1-p-nitrobenzyloxycarbonyl-2-(4-carboxybutyl)-4-acetylthiopyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04962103
Source datasetuspto-grants-1990_10
ORD IDord-b76b80c2e41a4ce9bb00875e3ccf3f5c
Source noteuspto-grants-1990_10