HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372418Generated: November 1, 2026
Sulfuric Acid → Diethyl 2-oxocyclohexane-1,1-dicarboxylate
https://huagongshe.com/reaction/2372418
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Ethyl 2-oxocyclohexanecarboxylate | HCID 95543 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl 2-oxocyclohexane-1,1-dicarboxylate | HCID 224023 | 109.6% |
| Product | HCID 178418443 | HCID 178418443 | — |
Reaction Steps
A tetrahydrofuran solution (30 ml) of ethylmagnesium bromide was prepared from bromoethane (7.05 g.) and magnesium (1.5 g.) The solution was cooled to 0° and 2-carbethoxycyclohexanone (10.0 g.) was added carefully. The reaction mixture was stirred at room temperature for 30 minutes and ethyl chloroformate (7.0 g.) was added dropwise, under nitrogen. A white precipitate developed. Sulphuric acid solution (80 ml, 1%) was added and the aqueous mixture was extracted with ether. The ether extracts were washed with dilute aqueous sodium hydrogen carbonate solution, water and then dried over anhydrous magnesium sulphate. The solvent was removed in vacuo. Distillation gave 2,2-dicarbethoxy-cyclohexanone (7.8 g.), a colourless oil, (b.pt. 98°-102° 0.9 mm.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05098929 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-da38a8d5c55a422ca760e581e75494a0 |
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| Source note | uspto-grants-1992_03 |
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