HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361886Generated: October 31, 2026
4-Hydroxycyclohexanecarboxylic acid → 1-(4-Hydroxycyclohexyl)ethanone
https://huagongshe.com/reaction/2361886
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxycyclohexanecarboxylic acid | HCID 151138 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Hydroxycyclohexyl)ethanone | HCID 13770153 | 42% |
Reaction Steps
Methyllithium (1M in THF) (120 mL, 3.5 eq.) was added to a solution of 4-hydroxy-cyclohexanecarboxylic acid (cis/trans mixture) (5.00 g, 1 eq.) in THF (350 mL) at −78° C. After stirring at −78° C. for 45 min, the cooling bath was removed and the resulting mixture was warmed to room temperature and stirred overnight. After total 24 h, the resulting reaction mixture was poured into ice/water (800 mL). This mixture was vigorously stirred. The separated aqueous phase was extracted with MeOH/EtOAc (˜1/20). The combined organic layer was dried over Na2SO4, filtered and concentrated. The crude product was purified by chromatography (50% to 100% EtOAc/hexanes) to give 1-(4-hydroxy-cyclohexyl)-ethanone (2.08 g, 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691814B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-ae87b9126d7c40779080b9b916682edf |
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| Source note | uspto-grants-2014_04 |
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