Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227745Generated: October 30, 2026

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

https://huagongshe.com/reaction/2227745

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 HC1, 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 numberUS06413991B1
Source datasetuspto-grants-2002_07
ORD IDord-2f7a8d84b4b2477fabfa933d1f3c8fc6
Source noteuspto-grants-2002_07