Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393949Generated: October 28, 2026

Carbon Dioxide → 5-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid

https://huagongshe.com/reaction/2393949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantTetrahydrofuranHCID 8028—
Reactant6-Bromo-2-tetralone ethylene ketalHCID 23377894—
ReactantHCID 178418306HCID 178418306—
Product5-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acidHCID 2818493—

Reaction Conditions

Temperature-78 °C

Reaction Steps

6-Bromo-2-tetralone ethylene ketal (2.2 g, 8.15 mmol) was dissolved in anhydrous THF (30 mL), cooled to -78° C. and treated with tert-butyllithium (12.05 mL, 20.4 mmol, 1.7M in pentane) under an atmosphere of nitrogen. After stirring for 30 minutes, anhydrous carbon dioxide gas was passed through the reaction mixture for 20 minutes at -78° C. The suspension was then allowed to warm to ambient temperature. The solution was quenched with water and acidified with 1N HCl, then extracted 2×EtOAc. The organic extracts were washed with brine, dried over Na2SO4 and concentrated in vacuo to a pale brown oil. The oily residue was applied to a silica flash chromatography column and eluted with 30%-50% EtOAC in hexanes to yield tetralone-6-carboxylic acid, ethylene ketal 1.06 g (55%) of a slowly crystallizing solid. NMR. MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05808080
Source datasetuspto-grants-1998_09
ORD IDord-08cba6c4f1fa4607a8b3728d61827d1a
Source noteuspto-grants-1998_09