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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972556Generated: October 30, 2026

Tributylphosphine → o-Methoxycarbonylbenzyltributylphosphonium bromide

https://huagongshe.com/reaction/972556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
ReactantMethyl 2-chloromethylbenzoateHCID 118590—
ReactantSodium BromideHCID 253881—
ReactantMethyl 2-(bromomethyl)benzoateHCID 2734813—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Producto-Methoxycarbonylbenzyltributylphosphonium bromideHCID 21388625—

Reaction Steps

To a suitable vessel containing about 16.2 g of an approximate 50:50 mixture of methyl α-chloro-o-toluate and methyl α-bromo-o-toluate is added 100 ml of acetonitrile and 17.2 g (0.085 mol) of tributylphosphine and held at reflux under nitrogen for about 45 minutes. The solvent is removed under vacuum and the residue is dissolved in 370 ml of water. The aqueous solution is extracted twice with ether and added to a solution of 102 g (1.0 mol) of sodium bromide in 150 ml of water. This mixture is extracted with three 150 ml portions of chloroform. The chloroform extracts are combined, dried over calcium sulfate and concentrated under vacuum to 36.3 g of colorless oil. Two triturations of this oil with ether provides a white solid which upon recrystallization from ethyl acetate-ether yields approximately 24.6 g of o-methoxycarbonylbenzyltributylphosphonium bromide having a melting point of 65°-66°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04053501
Source datasetuspto-grants-1977_10
ORD IDord-405fd26bf5b84149980f9811d3f73997
Source noteuspto-grants-1977_10