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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975640Generated: October 29, 2026

Triphenylphosphine → HCID 54275154, compound

https://huagongshe.com/reaction/975640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 53832192HCID 53832192—
ReactantHCID 178526132HCID 178526132—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 54275154HCID 54275154—

Reaction Steps

To a solution of (2R,4R)-1-allyloxycarbonyl-4-hydroxy-2-[3-(imidazol-1-yl)propyl]pyrrolidine (12.5 g) in tetrahydrofuran (125 ml) were added successively triphenylphosphine (17.6 g) and diethyl azodicarboxylate (10.6 ml) at -10° C. and the solution was stirred at the same temperature for 30 minutes. Then thiobenzoic acid (9.5 ml) was added at the same temperature and the solution was stirred for 3 hours. To the solution was added ethyl acetate (125 ml) and washed with saturated aqueous sodium hydrogen carbonate (125 ml×2) and brine (250 ml). The solution was dried over magnesium sulfate and the solvent was evaporated to give a yellow oil. The oil was chromatographed on a 500 g of silica gel to give (2R,4S)-1-allyloxycarbonyl-4-benzoylthio-2-[3-(imidazol-1-yl)propyl]pyrrolidine (15.3 g) as a yellow paste.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608056
Source datasetuspto-grants-1997_03
ORD IDord-a959da8058d74f169a773da0791f1ac4
Source noteuspto-grants-1997_03