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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069031Generated: October 29, 2026

Ammonium Chloride → 1-Phenoxy-3-vinylbenzene

https://huagongshe.com/reaction/1069031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-PhenoxybenzaldehydeHCID 38284—
ReactantTriphenylmethyl phosphonium bromideHCID 21951224—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product1-Phenoxy-3-vinylbenzeneHCID 983704171.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of triphenylmethylphosphonium bromide (25.23 g) and potassium tert-butoxide (1M solution in tetrahydrofuran) (75.67 ml) was stirred at 0° C. for 0.5 h. A solution of 3-phenoxy-benzaldehyde (10.0 g) in THF (10 ml) was added to the mixture and the reaction mixture stirred at 0° C. for 4 h. Ammonium chloride solution was added and the mixture extracted with diethyl ether. The organic extracts were combined, washed with water, dried and concentrated. Purification (SiO2, isohexane:ethyl acetate 4:1 as eluant) gave the subtitle compound (7.12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251910B1
Source datasetuspto-grants-2001_06
ORD IDord-be9fb439323f43619c9e52c210405015
Source noteuspto-grants-2001_06