Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450156Generated: October 25, 2026

Water → Methyl 2-(2-(benzyloxy)phenyl)-3-methoxyacrylate

https://huagongshe.com/reaction/1450156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(2'-benzyloxyphenyl)-3-hydroxyacrylateHCID 69942437—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(2-(benzyloxy)phenyl)-3-methoxyacrylateHCID 838698—
ProductMethyl 2-(2-(benzyloxy)phenyl)acetateHCID 11076055—

Reaction Steps

The crude methyl 2-(2'-benzyloxyphenyl)-3-hydroxyacrylate was dissolved in dry DMF (100 ml) and potassium carbonate (29.0 g) was added in one portion. Dimethyl sulphate (16.00 g) in dry DMF (10 ml) was then added dropwise with stirring. After ninety minutes, water (300 ml) was added and the solution was extracted with ether (2×300 ml). After washing with water (3×150 ml) and brine, the extracts were dried and concentrated under reduced pressure, and the resulting yellow oil solidified on trituration with ether/petrol. Recrystallization from dry methanol afforded (E)-methyl 2-(2'-benzyloxyphenyl) -3-methoxyacrylate as a white, crystalline solid (5.44 g, 17% yield from methyl 2-benzyloxyphenylacetate), mp. 76-77° C.; infrared max. (nujol mull): 1710, 1640 cm-1 ; 1H nmr (90 MHz): delta 3.63 (3H, s), 3.75 (3H, s), 5.05 (2H,s), 6.80-7.40 (9H,m), 7.50 (1H,s)ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602076
Source datasetuspto-grants-1997_02
ORD IDord-39baa328488a4f06a95cf95f93db7760
Source noteuspto-grants-1997_02