Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234182Generated: October 30, 2026

tert-Butyl acrylate → tert-Butyl 3-[2-(4-bromophenyl)ethoxy]propanoate

https://huagongshe.com/reaction/2234182

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acrylateHCID 15458—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant2-(4-Bromophenyl)ethanolHCID 72851—
Producttert-Butyl 3-[2-(4-bromophenyl)ethoxy]propanoateHCID 6913605266.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(4-Bromophenyl)ethanol (5 g) was treated with benzyltrimethylammonium hydroxide (Triton B®) (0.3 mL) and the resultant mixture was stirred in vacuo for 30 minutes. The mixture was then cooled to 0° C. and treated with t-butyl acrylate (3.5 g). The reaction was warmed to room temperature and stirred for 5 hours. The mixture was filtered through aluminium oxide (15 g) eluting with ether (75 mL). The collected filtrate was concentrated and purified by flash chromatography eluting with ethylacetate:iso-hexane (1:8) to give the sub-titled compound (5.42 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709511B2
Source datasetuspto-grants-2010_05
ORD IDord-439c951efb204572a5b85acff77ebe64
Source noteuspto-grants-2010_05