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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258112Generated: November 3, 2026

Triphenylphosphine → S-(1-(4,5-dihydrothiazol-2-yl)azetidin-3-yl) ethanethioate

https://huagongshe.com/reaction/2258112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant1-(4,5-Dihydrothiazol-2-yl)azetidin-3-olHCID 10986515—
ReactantHCID 178418634HCID 178418634—
SolventTetrahydrofuranHCID 8028—
ProductS-(1-(4,5-dihydrothiazol-2-yl)azetidin-3-yl) ethanethioateHCID 1179061965%

Reaction Steps

There were added 119 mg of 3-hydroxy-1-(1,3-thiazolin-2-yl)azetidine (6) and two molar equivalents of thioacetic acid, while cooled with ice, to 10 ml of tetrahydrofuran solution containing two molar equivalents of triphenylphosphine and two molar equivalents of diethylazodicarboxylate, and the resultant solution was stirred for one hour at the same temperature, and for further one hour at a room temperature. The solvent of the reaction liquid was evaporated in a vacuum, and the obtained residue was subjected to silica gel column chromatography (eluent: chloroform-ethanol), and, thus, there was obtained 107 mg (yield: 65%) of 3-acetylthio-1-(1,3-thiazolin-2-yl)azetidine (7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05659043
Source datasetuspto-grants-1997_08
ORD IDord-75aa402e56ea4304993e1a1a5a7b8475
Source noteuspto-grants-1997_08