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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066809Generated: October 30, 2026

Triphenylphosphine → HCID 59409878, compound

https://huagongshe.com/reaction/2066809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 59409882HCID 59409882—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59409878HCID 5940987882%

Reaction Steps

A mixture of (5S)-5-(azidomethyl)-3-(5-chloropyridin-2-yl)-1,3-oxazolidin-2-one (2.31 g, INTERMEDIATE 8) and triphenylphosphine (3.58 g) was heated to 65° C. for 6 h in 444 ml of tetrahydrofuran and 56 ml of water. The sample was then cooled to room temperature, and concentrated in vacuo. The residue was purified via column chromatography on a Biotage Horizon 40M column eluting with 100% ethyl acetate (5 column volumes) to remove excess triphenylphosphine and triphenylphosphine oxide, followed by 100% methanol (5 column volumes), to provide the title compound (1.70 g, 82%). Mass spectrum (ESI) 228.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293721B2
Source datasetuspto-grants-2012_10
ORD IDord-f7440259c820422caede738998c4c332
Source noteuspto-grants-2012_10