HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888272Generated: October 31, 2026
1-Ethynylcyclohexanol → HCID 58399442, compound
https://huagongshe.com/reaction/888272
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethynylcyclohexanol | HCID 6525 | — |
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58399442 | HCID 58399442 | 61% |
Reaction Steps
To a solution of 1-ethynylcyclohexanol (500 mg, 4.02 mmol) in tetrahydrofuran (20 mL), 2.77 M n-butyllithium (solution in n-hexane, 3.6 mL, 9.90 mmol) was added dropwise at −78° C., and the obtained solution was stirred at the same temperature for 1 hour. To the reaction solution, p-tolualdehyde (0.52 mL, 4.40 mmol) was added at −78° C., and the obtained solution was allowed to warm gradually to room temperature with stirring. To the reaction solution, distilled water and 1 M hydrochloric acid were added to make the mixture acidic, and the resultant was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, n-hexane/ethyl acetate) to obtain the captioned compound (598 mg, 2.44 mmol, 61%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247569B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-abb15a84d94045f5bb8c828b7cebbb3b |
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| Source note | uspto-grants-2012_08 |
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