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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194785Generated: October 27, 2026

Phosphine, triphenyl-, hydrobromide → [1-(4,5,6,7-Tetrahydro-4,4,7,7-tetramethylbenzo-[b]thien-2-yl)ethyl]triphenylphosphonium bromide

https://huagongshe.com/reaction/1194785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphine, triphenyl-, hydrobromideHCID 517696—
Reactant4,5,6,7-Tetrahydro-alpha,4,4,7,7-pentamethylbenzo[b]thiophene-methanolHCID 86740244—
SolventAcetonitrileHCID 6342—
Product[1-(4,5,6,7-Tetrahydro-4,4,7,7-tetramethylbenzo-[b]thien-2-yl)ethyl]triphenylphosphonium bromideHCID 23049224103.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

20.2 g of 4,5,6,7-tetrahydro-α,4,4,7,7-pentamethylbenzo[b]thiophene-methanol are dissolved in 260 ml of acetonitrile and the solution is treated with 29.2 g of triphenylphosphonium bromide. After stirring at 50° C. for 3 hours, the mixture is evaporated to dryness, the residue is taken up with 80% aqueous ethanol and extracted twice with hexane. The ethanol phase is evaporated, the residue is dissolved in methylene chloride, the solution is dried over sodium sulphate and evaporated. There are obtained 49.4 g of [1-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)ethyl]triphenylphosphonium bromide as an amorphous white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816476
Source datasetuspto-grants-1989_03
ORD IDord-8a716cf9a7f84464858b1a5c892c753e
Source noteuspto-grants-1989_03