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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990710Generated: October 31, 2026

Triphenylphosphine → HCID 67396730, compound

https://huagongshe.com/reaction/1990710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2,4-OxazolidinedioneHCID 97389—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 67396768HCID 67396768—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 67396730HCID 6739673079.5%

Reaction Steps

0.4 ml of a 40% solution of diethyl azodicarboxylate (0.9 mmol) in toluene is added to a solution, cooled with an ice bath, of 0.111 g (0.44 mmol) of 3-[6-(4-chlorophenyl)pyrimidin-4-yl]propan-1-ol, prepared in stage 5.4., of 0.077 g (0.76 mmol) of 1,3-oxazolidine-2,4-dione and of 0.235 g (0.89 mmol) of triphenylphosphine in 4 ml of tetrahydrofuran. The mixture is subsequently stirred at ambient temperature overnight. It is taken up in a mixture of ethyl acetate and of water. The organic phase is washed with a saturated aqueous sodium chloride solution, dried over sodium sulphate and evaporated. The residue is purified by chromatography on silica gel, elution being carried out with a 97/3 mixture of dichloromethane and of methanol, to produce 0.117 g (0.35 mmol) of product in the solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645757B2
Source datasetuspto-grants-2010_01
ORD IDord-b3d365e1b1e54821b1d92847d8a57496
Source noteuspto-grants-2010_01