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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072712Generated: November 1, 2026

Triphenylphosphine → Triphenylphosphine Oxide

https://huagongshe.com/reaction/2072712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 15676007HCID 15676007—
SolventCarbon TetrachlorideHCID 5943—
ProductTriphenylphosphine OxideHCID 13097—

Reaction Steps

To 3-(2-fluoro-4-biphenylyl)-2-oxo-1-butanol (2.00 g, 7.74 mmol) in carbon tetrachloride (5 ml) was added triphenylphosphine (2.15 g, 8.20 mmol) at room temperature. After the addition, the mixture was stirred over night at room temperature, then concentrated to give triphenylphosphine oxide as precipitates. After filtration of the precipitates, the filtrates were evaporated under reduced pressure to a residue, which was chromatographed to afford 1-chloro-3-(2-fluoro-4-biphenylyl)-2-butanone (1.01 g, 47% yield) as crystalline materials: mp 57°-59° C.; NMR(CDCl3)δ 1.48(d, 3H), 4.07(m, 3H), 6.93-7.63(m, 8H); IR(neat) 1740, 1620, 1480, 1420, 1270 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914112
Source datasetuspto-grants-1990_04
ORD IDord-5b13f7b0d4ae4017878bd69cc4dfe3d2
Source noteuspto-grants-1990_04