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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 6-Bromo-2-tetralone ethylene ketal | HCID 23377894 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Product | 5-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid | HCID 2818493 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05808080 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-08cba6c4f1fa4607a8b3728d61827d1a |
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| Source note | uspto-grants-1998_09 |
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