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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225030Generated: October 31, 2026

2,3-Dichloropropene → 7-[(2-Chloroprop-2-en-1-yl)oxy]-4,8-dimethyl-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/225030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichloropropeneHCID 6565—
ReactantPotassium CarbonateHCID 11430—
Reactant2H-1-Benzopyran-2-one, 7-hydroxy-4,8-dimethyl-HCID 5356597—
SolventAcetoneHCID 180—
Product7-[(2-Chloroprop-2-en-1-yl)oxy]-4,8-dimethyl-2H-1-benzopyran-2-oneHCID 1320805977%

Reaction Steps

A mixture of 4,8-dimethyl-7-hydroxycoumarin (8.00 g., 42.1 m mole); anhydrous potassium carbonate (18.1 g., 130 m mole); 2,3-dichloropropene (33.6 g., 302 m mole); and acetone (600 ml.) was stirred and heated under reflux for twenty-four hours. The reaction mixture was concentrated to ca. 200 ml., filtered, and the inorganic salts were washed with acetone. Evaporation of the combined filtrate and washing under reduced pressure left a tan-colored residue (11.30 g.). Recrystallization from aqueous methanol gave a 77% yield of 4,8-dimethyl-7-(2'-chloroallyloxy)coumarin as small, off-white needles (8.55 g., m.p. 117.5°-120° C.). Another recrystallization did not change the m.p. but gave an analytical sample.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235781
Source datasetuspto-grants-1980_11
ORD IDord-47550ce385624156a845ad3e3d4f4a1a
Source noteuspto-grants-1980_11