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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706457Generated: November 1, 2026

Chloroform → 4-Benzyloxy-7-(2-[4-fluorophenyl]ethoxy)coumarin

https://huagongshe.com/reaction/1706457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluorophenethyl bromideHCID 573153—
Reactant4-Benzyloxy-7-hydroxycoumarinHCID 13408407—
SolventAcetoneHCID 180—
Product4-Benzyloxy-7-(2-[4-fluorophenyl]ethoxy)coumarinHCID 22751306—

Reaction Steps

A mixture of 4-benzyloxy-7-hydroxycoumarin (5.36; 0.02 mole) anhydrous potassium carbonate (4.0 g) and 1-bromo-2-(4-fluorophenyl) ethane (4.06 g) in acetone (100 ml) was stirred at reflux for 20 hours and the inorganic material filtered off. Evaporation of the filtrate in vacuo gave an oil which rapidly set solid on scratching. Chloroform (200 ml) was added and the mixture filtered to remove unchanged 4-benzyloxy-7-hydroxycoumarin. Reevaporation of the filtrate afforded a white solid, 3.34 g (43%) of m.p. 120°, νmax (mull) 1715, 1675, 1620 cm-1 ; τ(CDCl3); 6.93 (2H, t, J 6.7 Hz); 5.80 (2H, t, J 6.7 Hz); 4.87 (2H,S); 4.38 (1H,); 3.29-2.49 (6H, m) 2.32 (1H, d, J 10 Hz); (Found C, 73.75 H, 5.14 C24H19FO4 requires; C, 73.84; H, 4.91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207335
Source datasetuspto-grants-1980_06
ORD IDord-f5ecc34535f14491aea18c4614b43da0
Source noteuspto-grants-1980_06