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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566258Generated: October 31, 2026

Triphenylphosphine → HCID 21265833, compound

https://huagongshe.com/reaction/566258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant2-(1-Methyl-1H-imidazol-2-yl)ethanolHCID 565964—
ReactantHCID 178526132HCID 178526132—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 21265833HCID 21265833—

Reaction Steps

Triphenylphosphine (10.48 g) was dissolved in tetrahydrofuran (120 ml). To the solution were added diisopropyl azodicarboxylate (8.07 g) at 0° C. The mixture was stirred for 15 minutes at the same temperature. To the mixture were added a solution of 2-(1-methyl-2-imidazolyl)ethanol (2.52 g) in tetrahydrofuran (10 ml) and thiobenzoic acid (4.7 ml) in the order mentioned. The mixture was stirred for 2.5 hours at 0° C. and then for 1 hour at room temperature. The reaction mixture was diluted with ethyl acetate, then washed with saturated solution of sodium hydrogencarbonate in water and saturated solution of sodium chloride in water in the order mentioned. The residue was dried over anhydrous sodium sulfate and concentrated under reduced pressure, which was then subjected to column chloromatography on silica gel (developing solvent: ethyl acetate-methanol: 100:0→93:7) to give the title compound (3.52 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174877B1
Source datasetuspto-grants-2001_01
ORD IDord-867da67d95bc4106969ff4498f5849da
Source noteuspto-grants-2001_01