HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58891Generated: October 30, 2026
Ammonium Chloride → Ethyl 4-hydroxy-4-methylcyclohexane-1-carboxylate
https://huagongshe.com/reaction/58891
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 4-oxocyclohexanecarboxylate | HCID 317638 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 4-hydroxy-4-methylcyclohexane-1-carboxylate | HCID 21911966 | 41% |
Reaction Steps
To a solution of ethyl 4-oxocyclohexanecarboxylate (4.00 g, 23.5 mmol) in diethyl ether (80 mL) was added MeLi (37.6 mL, 1M in diethyl ether) at −60° C. under nitrogen atmosphere. The reaction mixture was stirred at −60° C. for 30 min. Saturated aqueous NH4Cl (50 mL) was added and the resulting mixture was extracted with EtOAc (100 mL×2). The combined organic layers were washed with brine (150 mL) and water (150 mL), dried over anhydrous sodium sulfate, and concentrated. The residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=10:1) to afford ethyl 4-hydroxy-4-methylcyclohexanecarboxylate (1.8 g, 41% yield) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434761B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-5683a11f2fe443e6839b40159d080476 |
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| Source note | uspto-grants-2016_09 |
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