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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731564Generated: October 25, 2026

Triphenylphosphine → Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester

https://huagongshe.com/reaction/1731564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl bromoacetateHCID 60984—
ReactantPhosphonium, (2-methoxy-2-oxoethyl)triphenyl-, bromide (1:1)HCID 2733211—
ReactantPhosphoniumHCID 5460504—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 1745380%

Reaction Conditions

Temperature70 °C

Reaction Steps

Triphenyl phosphine (13 g.) was dissolved in dry benzene (60 ml.) and methyl bromoacetate (8.3 g.) was added dropwise. The solution was heated at 70° C., for 2 days, and then cooled and filtered. The residue was washed with benzene and dried to give about 16 g. of (methoxycarbonyl methyl)triphenylphosphonium bromide. The phosphonium salt (10 g.) was dissolved in water (250 ml.) and 5% aqueous sodium hydroxide was added dropwise with stirring until the solution became alkaline to litmus. The resulting precipitate was filtered off, washed with water and dried. Crystallisation from ethyl acetate/petroleum spirit gave (methoxycarbonyl methylene) triphenyl phosphorane as a colourless solid in about 80% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04622337
Source datasetuspto-grants-1986_11
ORD IDord-3476553ebdfe4c05b6d48784eacaf486
Source noteuspto-grants-1986_11