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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265982Generated: October 27, 2026

Ethyl vinyl ether → 2-Bromo-4-(1-ethoxy-ethoxy)-but-1-ene

https://huagongshe.com/reaction/1265982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl vinyl etherHCID 8023—
Reactant3-Bromo-3-buten-1-olHCID 533975—
CatalystTriethylamineHCID 8471—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventDiethyl EtherHCID 3283—
Product2-Bromo-4-(1-ethoxy-ethoxy)-but-1-eneHCID 1854820791.6%

Reaction Steps

While cooling a solution of 10.38 g (0.0687 mol) of 3-bromo-3-buten-1-ol in 20 ml of diethyl ether with 50 mg (0.000263 mol) p-toluene sulfonic acid monohydrate in an ice water bath, 19 ml (0.199 mol) of ethyl vinyl ether was added slowly dropwise to maintain an internal temperature of <10° C. After 1 hour at 0° C., a few drops of triethylamine was added. The reaction mixture was poured onto water. The resulting mixture was transferred to a separatory funnel and the phases were separated. The isolated organic layer was washed with brine then dried over potassium carbonate and filtered. The solvent was removed from the filtrate in vacuo to yield 14.04 g of 2-bromo-4-(1-ethoxy-ethoxy)-but-1-ene as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548448B2
Source datasetuspto-grants-2003_04
ORD IDord-76ebaf9507254ae199d91d59c0e642b1
Source noteuspto-grants-2003_04