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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034494Generated: October 31, 2026

Hydrochloric Acid → HCID 57126089, compound

https://huagongshe.com/reaction/1034494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium ethanethioateHCID 23670855—
ReactantHCID 57239737HCID 57239737—
SolventDimethylformamideHCID 6228—
ProductHCID 57126089HCID 5712608974.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of (2S,4R)-1-t-butoxycarbonyl-2-phthalimidomethyl-4-methanesulfonyloxypyrrolidine (3 g) in dimethylformamide (30 ml), potassium thioacetate (1.65 g) is added. The mixture is stirred at 60° C. for 3.5 hours. The reaction mixture is poured into a mixture of ethyl acetate and dilute hydrochloric acid. The organic layer is taken, washed with water, dried over sodium sulfate, and concentrated in vacuo. The residue is purified by silica gel column chromatography to give (2S,4S)-1-t-butoxycarbonyl-2-phthalimidomethyl-4-acetylthiopyrrolidine (2.12 g). Yield: 74%. Orange colored syrup. NMR δ(CDCl3) ppm: 1.30, 1.39(2×s, 9H), 1.6 to 2.0(m, 1H), 2.34(s, 3H), 2.4 to 2.67(m, 1H), 3.15 to 3.3(m, 1H), 3.65 to 4.55(m, 5H), 7.6 to to 8.0(m, 4H). IR ν (CHCl3) cm-1 : 1774, 1715, 1688.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05317016
Source datasetuspto-grants-1994_05
ORD IDord-1dde467375f84b3c8923bce66467af17
Source noteuspto-grants-1994_05