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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066803Generated: November 2, 2026

Triphenylphosphine → HCID 59409914, compound

https://huagongshe.com/reaction/2066803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 59409897HCID 59409897—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59409914HCID 5940991497.8%

Reaction Steps

A mixture of 5-(azidomethyl)-3-(5-chloropyridin-2-yl)-1,3-oxazolidin-2-one (139 mg, INTERMEDIATE 2) and triphenylphosphine (226 mg) was heated to 65° C. for 8 h in 66 ml of tetrahydrofuran and 9 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 (122 mg, 94%). Mass spectrum (ESI) 228.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293721B2
Source datasetuspto-grants-2012_10
ORD IDord-d0d8a902efe745398b0253326b302a76
Source noteuspto-grants-2012_10