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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374344Generated: October 25, 2026

2-Methoxyethanol → tert-Butyl 2-(2-methoxyethoxymethyl)acrylate

https://huagongshe.com/reaction/374344

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 2-(bromomethyl)prop-2-enoateHCID 10955115—
SolventWaterHCID 962—
Producttert-Butyl 2-(2-methoxyethoxymethyl)acrylateHCID 11096016—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 2-(bromomethyl)acrylate (2.0 g, 9.0 mmol) in 2-methoxyethanol (30 ml) at 0° C. was added, in one portion, potassium carbonate (2.5 g, 18 mmol) and the mixture stirred at 0° C. for 1 hour. The reaction was diluted with distilled water (100 ml) and extracted with dichloromethane (100 ml). The layers were separated and the aqueous layer further extracted with dichloromethane (2×50 ml). The combined organic extracts were dried over magnesium sulphate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on silica by eluting with hexane/ethyl acetate (2:1) to give, after combination and evaporation of appropriate fractions, the title compound as a yellow oil, (1.6 g, 82%). Rf. 0.32 (silica, hexane/ethyl acetate, 2:1). 1H-NMR (300 MHz, CDCl3) 1.50 (s, 9H), 3.42 (s, 3H) , 3.56-3.63 (m, 2H), 3.65-3.74 (m, 2H), 4.25 (s, 2H), 5.84 (s, 1 H), 6.25 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166406
Source datasetuspto-grants-1992_11
ORD IDord-06bbc94676984a0b90ae259620110917
Source noteuspto-grants-1992_11