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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443763Generated: October 31, 2026

Triphenylphosphine → HCID 86226740, compound

https://huagongshe.com/reaction/1443763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-benzylazetidin-3-olHCID 3801345—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 178418634HCID 178418634—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86226740HCID 8622674084.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triphenylphosphine (3.08 g, 11.76 mmol) was dissolved in anhydrous tetrahydrofuran (THF) (30 ml). Oxygen was completely removed by passing nitrogen through the mixture, and the mixture was cooled to 0° C. Diisopropylazodicarboxylate (2.3 ml, 11.76 mmol) was added thereto, and stirred at 0° C. for 1 hour. Added slowly to the mixture in succession were thioacetic acid (840 μl, 11.76 mmol) and 1-benzyl-azetidine-3-ol (960 mg, 5.88 mmol) prepared in Preparation Example 37 and dissolved in tetrahydrofuran (20 ml). The resulting solution was heated to room temperature, stirred for 2 hours and concentrated under a reduced pressure to remove the solvent. The concentrate was dissolved in ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and concentrated under a reduced pressure. The resulting residue was purified by column chromatography (eluent−ethyl acetate/normal hexane=1/1) to obtain 1.1 g (yield: 83%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662810B2
Source datasetuspto-grants-2010_02
ORD IDord-0fb11e2264cb44f3870b8874d597c7dd
Source noteuspto-grants-2010_02