HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353468Generated: October 27, 2026
Hydrochloric Acid → 1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid
https://huagongshe.com/reaction/353468
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyclohexanecarboxylic acid | HCID 7413 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Pentane, 3-(bromomethyl)- | HCID 77432 | — |
| Reactant | Lithium isopropylamide | HCID 10877046 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | 1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid | HCID 10488751 | 64% |
Reaction Steps
A suspension of 60% sodium hydride (980 mg) in tetrahydrofuran (80 ml) was stirred at room temperature and a tetrahydrofuran solution (10 ml) containing cyclohexanecarboxylic acid (3.00 g) was added dropwise thereto. After completion of addition, a mixture was stirred for 1 hour and cooled to 0° C., followed by adding a cyclohexane solution (18.7 ml) containing 1.5 M lithium isopropylamide dropwise thereto. Then, after stirring at room temperature for 1.5 hours and cooling to 0° C., a tetrahydrofuran solution (10 ml) containing 1-bromo-2-ethylbutane (4.64 g) was added dropwise thereto. The solution was gradually warmed to room temperature and stirred overnight. Water and a 10% hydrochloride solution were added to this reaction solution and the solution was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. After drying, the resulting solution was concentrated to obtain 1-(2-ethylbutyl)cyclohexanecarboxylic acid (3.17 g, yield: 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06753346B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-ce1d467411124cf3b5a5d1ccaa53df3b |
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| Source note | uspto-grants-2004_06 |
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