Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671729Generated: October 26, 2026

Triphenylphosphine → 2E-5-trimethylsilylpent-2-en-4-ynyltriphenylphosphonium bromide

https://huagongshe.com/reaction/1671729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-Bromo-5-trimethylsilylpent-2-en-4-yneHCID 57280803—
SolventTolueneHCID 1140—
Solventtert-Butyl methyl etherHCID 15413—
Product2E-5-trimethylsilylpent-2-en-4-ynyltriphenylphosphonium bromideHCID 1115585180.8%

Reaction Steps

Triphenylphosphine (64.1 g, 0.244 mol) was added to a solution of 1-bromo-5-trimethylsilylpent-2-en-4-yne (44.26 g, 0.204 mol) in toluene (204 mL). The mixture was stirred at ambient temperature under a nitrogen atmosphere. After 3 days the suspension was diluted with methyl tert-butyl ether (408 mL), stirred for 1 hour at ambient temperature, and the precipitate was collected by filtration. The filter cake was washed with methyl tert-butyl ether and dried under vacuum at 30° C. to get 79 g of 2E-5-trimethylsilylpent-2-en-4-ynyltriphenylphosphonium bromide, a compound of formula (Q), as an off-white powder: 1H-NMR (300 mHz, CDCl3) 6 0.14 (s, 9H), 5.08 (dd, 2H), 5.91 (dt, 1H), 6.22 (dd, 1H), 7.6-8.0 (m, 15 H); Anal. Calculated for C26H28BrPSi requires C 65.13, H 5.89, Br 16.66, P 6.46; found C 64.95, H 5.78, Br 16.96, P 6.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994346B2
Source datasetuspto-grants-2011_08
ORD IDord-b8202acdd00a40d4b0c2d96ac67c16e6
Source noteuspto-grants-2011_08