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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471445Generated: October 30, 2026

Triphenylphosphine → HCID 86703885, compound

https://huagongshe.com/reaction/471445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Bromo-3,5-dimethylphenolHCID 81970—
ReactantDi-tert-butyl diazene-1,2-dicarboxylateHCID 6034084—
Reactant1427028-11-2HCID 57578793—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86703885HCID 86703885—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-bromo-3,5-dimethylphenol, (306 mg, 1.52 mmol), (1-Methanesulfonyl-cyclopropyl)-methanol (228 mg, 1.52 mmol), and triphenylphosphine (399 mg, 1.52 mmol) are suspended in dry tetrahydrofuran (10 mL) and cooled to 0° C. Di-tert-butylazodicarboxylate (350 mg, 1.52 mmol) is added and the mixture stirred at 50° C. for 48 hours then at room temperature for a further 48 hours. The mixture is concentrated under vacuum then partitioned between water and dichloromethane, The organic phase is dried and the solvent removed under vacuum. The residue is purified by flash chromatography (0-20% ethyl acetate in cyclohexane) to give the title compound as a crude material which was used without further purification (Yield 664 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633182B2
Source datasetuspto-grants-2014_01
ORD IDord-39753b914b4b445ab38229b114cac4de
Source noteuspto-grants-2014_01