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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086993Generated: October 26, 2026

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

https://huagongshe.com/reaction/1086993

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 3-hydroxy-2-(2'-benzyloxyphenyl)propenoate 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 x 300 ml). After washing with water (3 x 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 3-methoxy-2-(2'-benzyloxyphenyl)propenoate as a white, crystalline solid (5.44g, 17% yield from methyl 2-benzyloxyphenylacetate), M.P. 76-77° C.; infrared maxima (nujol mull): 1710, 1640 cm-1 ; 1H nmr (CDCl3, 90MHz): 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 numberUS05034388
Source datasetuspto-grants-1991_07
ORD IDord-a1c0d762440c4a9c8b15d14b0891577c
Source noteuspto-grants-1991_07