Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435857Generated: October 30, 2026

Benzyltrimethylammonium hydroxide → 6-[2-hydroxy-3-(2-propylphenoxy)propoxy]-4-oxo-4H-1-benzopyran-2-carboxylic acid

https://huagongshe.com/reaction/435857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantSodium BicarbonateHCID 516892—
Reactant4H-1-Benzopyran-2-carboxylic acid, 6-hydroxy-4-oxo-, ethyl esterHCID 616464—
Reactant1,2-Epoxy-3-(2-propylphenoxy)propaneHCID 12355851—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-[2-hydroxy-3-(2-propylphenoxy)propoxy]-4-oxo-4H-1-benzopyran-2-carboxylic acidHCID 13090998—

Reaction Steps

A mixture of 19.2 parts of 1,2-epoxy-3-(2-propylphenoxy) propane, 23.4 parts of ethyl 6-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylate and 0.1 parts of benzyl trimethylammonium hydroxide in 50 parts of dimethyl formamide was heated under reflux for 3 hours. The solvent was evaporated under reduced pressure and the oil remaining dissolved in ethyl acetate. The solution was washed with dilute sodium hydroxide and water, dried over magnesium sulphate, filtered and evaporated to leave an oil. The oil was dissolved in ethyl alcohol, 20.0 parts of sodium bicarbonate were added, and the mixture was boiled for 2 hours, during which time water was added and the ethyl alcohol allowed to boil off. The aqueous solution was washed with ethyl acetate and acidified with dilute hydrochloric acid to give a brown precipitate which was collected and crystallised twice from ethyl alcohol to yield 10.5 parts of 6-[2-hydroxy-3-(2-propylphenoxy)propoxy]-4-oxo-4H-1-benzopyran-2-carboxylic acid, melting point 164°-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006245
Source datasetuspto-grants-1977_02
ORD IDord-6b16b91801814526ac9e6f27c279cc31
Source noteuspto-grants-1977_02