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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066819Generated: November 1, 2026

Triphenylphosphine → HCID 59409859, compound

https://huagongshe.com/reaction/2066819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 59409876HCID 59409876—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59409859HCID 5940985988,800.102%

Reaction Steps

A mixture of 5-(azidomethyl)-3-(5-chloropyridin-2-yl)-5-methyl-1,3-oxazolidin-2-one (570 mg, INTERMEDIATE 18) and triphenylphosphine (1.12 g) was heated to 65° C. for 4 h in 80 ml of tetrahydrofuran and 10 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 (4 column volumes) to remove excess triphenylphosphine and triphenylphosphine oxide, followed by 100% methanol (4 column volumes), to provide the title compound (457 g, 89%). Mass spectrum (ESI) 242.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293721B2
Source datasetuspto-grants-2012_10
ORD IDord-4104da69f9c742d4bec90ef4cc5f63bd
Source noteuspto-grants-2012_10