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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833295Generated: October 31, 2026

o-Toluate → o-Propoxycarbonylbenzyltributylphosphonium bromide

https://huagongshe.com/reaction/1833295

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-ToluateHCID 6997338—
Reactant2-Bromomethylbenzoyl chlorideHCID 12251632—
ReactantPropyl alpha-chloro-o-toluateHCID 18464439—
ReactantPropyl alpha-bromo-o-toluateHCID 21388617—
Reactanto-Methoxycarbonylbenzyltributylphosphonium bromideHCID 21388625—
Solvent1-PropanolHCID 1031—
Producto-Propoxycarbonylbenzyltributylphosphonium bromideHCID 21388593—

Reaction Steps

Using the procedure of Example V, but substituting a mixture of propyl α-chloro-o-toluate and propyl α-bromo-o-toluate, prepared from propyl alcohol and α-bromo-o-toluoyl chloride, for the toluate mixture of Example V provides an oil which upon triturating several times with ether and precipitating as an oil from ethyl acetate with ether and drying yields 18.7 g of o-propoxycarbonylbenzyltributylphosphonium bromide, an oil having a structure in accordance with formula (1) which is confirmed by nmr spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066435
Source datasetuspto-grants-1978_01
ORD IDord-36d545d8841c4e0e88fba35ecc7663ed
Source noteuspto-grants-1978_01