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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675331Generated: October 28, 2026

Triphenylphosphine → HCID 86634599, compound

https://huagongshe.com/reaction/1675331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(3,4-Dichloroisothiazol-5-yl)methanolHCID 16723166—
ReactantHCID 178418634HCID 178418634—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86634599HCID 8663459932%

Reaction Steps

To a THF (50 ml) solution of 2.85 g (10.9 mmol) of triphenylphosphine was added, under ice-cooling, 2.2 g (10.9 mmol) of diisopropyl azodicarboxylate, followed by stirring for 30 minutes. To the solution was added a THF (5 ml) solution of 1.0 g (5.43 mmol) of (3,4-dichloroisothiazol-5-yl)methanol and 0.83 g (10.9 mmol) of thioacetic acid, followed by stirring at room temperature for 5 hours, to give rise to a reaction. After the completion of the reaction, ethyl acetate was added to the reaction mixture. The resulting mixture was washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography to obtain 0.42 g (yield: 32%) of (3,4-dichloroisothiazol-5-yl)methyl thioacetate as a light red oily substance (refractive index: 1.5855).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003675B2
Source datasetuspto-grants-2011_08
ORD IDord-361b4fe5c1f04d3aaa38dd7b0bd04dc1
Source noteuspto-grants-2011_08