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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912430Generated: October 30, 2026

Triphenylphosphine → HCID 58293300, compound

https://huagongshe.com/reaction/1912430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium ThiosulfateHCID 24477—
ReactantOzoneHCID 24823—
ReactantHCID 58293397HCID 58293397—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventChloroform methanolHCID 21584188—
ProductHCID 58293300HCID 58293300—

Reaction Steps

A solution of an optically-active compound of 3-methyl-2-(3-methyl-but-2-enyl)-azetidine-1,2-dicarboxylic acid di-tert-butyl ester (44.5 g) in chloroform/methanol (310 ml/310 ml) cooled to −70° C. was flowed ozone air for 1 hour. To the reaction mixture was added a solution of triphenylphosphine (44.7 g) in chloroform (45 ml) in small batches, and the mixture was warmed to room temperature. To the mixture were added saturated aqueous sodium thiosulfate solution (200 ml) and water (300 ml), and the mixture was extracted with chloroform (500 ml). The separated organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give the titled compound (95.0 g), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609647B2
Source datasetuspto-grants-2013_12
ORD IDord-cae50defd50249019f4e3cce7ddf57c6
Source noteuspto-grants-2013_12