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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169352Generated: November 4, 2026

Carbon Dioxide → 3-(4-methylphenyl)-2H-1-benzopyran-6-carboxylic acid

https://huagongshe.com/reaction/1169352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
Reactant6-bromo-3-(4-methylphenyl)-2H-1-benzopyranHCID 22990132—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-(4-methylphenyl)-2H-1-benzopyran-6-carboxylic acidHCID 22990128—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Into a solution of 6-bromo-3-(4-methylphenyl)-2H-1-benzopyran (0.5 g) in THF (15 ml) was added at −78° C. 1.6 M butyl lithium (a hexane solution) (1.14 ml) under a nitrogen atmosphere. The resulting mixture was stirred at −78° C. for one hour, was then mixed with dry ice and was stirred for additional one hour. After addition of 1 N hydrochloric acid (10 ml), the resulting mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated solution of sodium chloride and was dried with magnesium sulfate. After concentration under reduced pressure, the resulting crystals were collected by filtration, and the crystals were washed with diethyl ether and hexane to obtain 3-(4-methylphenyl)-2H-1-benzopyran-6-carboxylic acid (218 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627651B1
Source datasetuspto-grants-2003_09
ORD IDord-a7c9f4bc7cf1419f8ffeeeb820bb018c
Source noteuspto-grants-2003_09