Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249607Generated: October 28, 2026

Triphenylphosphine → Phosphonic dichloride, (2-methylphenyl)-

https://huagongshe.com/reaction/1249607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantPhosphonic dichloride, (2-methylphenyl)-HCID 10921725—
ProductPhosphonic dichloride, (2-methylphenyl)-HCID 10921725—
ProductPhosphonous dichloride, (2-methylphenyl)-HCID 14226801—

Reaction Steps

317 g (1.52 moles) of o-tolylphosphonic acid dichloride and 400 g (1.53 moles) of triphenylphosphane were stirred for 17 hours at 180° C. under an atmosphere of nitrogen. The mixture was then cooled and the triphenylphosphane oxide which had crystallized out was filtered off with suction. The filtrate was distilled at 0.093 kPa at a top temperature of approx. 80°-100° C. This gave 220 g, containing 45% of dichloro-o-tolylphosphane and 45% of o-tolylphosphonic acid dichloride (according to 31P-NMR spectrum). The dichloro-o-tolylphosphane was obtained at a yield of 50% of theory, at a 68.5% conversion of o-tolylphosphonic acid dichloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04632995
Source datasetuspto-grants-1986_12
ORD IDord-e7590209ead8497b82555773e233545d
Source noteuspto-grants-1986_12