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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050161Generated: October 30, 2026

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

https://huagongshe.com/reaction/2050161

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 (4.0g) and 1-bromo-2-(4-fluorophenyl) ethane (4.06g) in acetone (100ml) 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 (200ml) was added and the mixture filtered to remove unchanged 4-benzyloxy-7-hydroxycoumarin. Reevaporation of the filtrate afforded a white solid, 3.34g (43%) of m.p. 120°, νmax (mull) 1715, 1675, 1620cm-1 ; τ(CDCl3); 6.93 (2H, t, J 6.7 Hz); 5.80 (2H, t, J 6.7 Hz); 4.87 (4.38 (1H,); 3.29-2.49 (6H, m) 2.32 (1H, d, J 10Hz); (Found C, 73.75 H, 5.14C24H19FO4 requires; C. 73.84; H, 4.91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200577
Source datasetuspto-grants-1980_04
ORD IDord-8f9b698f0e004e59940ecbefc1205ba3
Source noteuspto-grants-1980_04