HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295627Generated: October 26, 2026
1-Methylcyclohexanecarboxylic acid → (1-Methylcyclohexyl)methanol
https://huagongshe.com/reaction/1295627
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylcyclohexanecarboxylic acid | HCID 70744 | — |
| Reactant | Diboron | HCID 6328200 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-Methylcyclohexyl)methanol | HCID 1501840 | 69% |
Reaction Steps
To a solution of 1-methyl-1-hydroxycarbonylcyclohexane (10 g, 70 mmol) in tetrahydrofuran(300 mL) at 0° C. was added 1M diborane in tetrahydrofuran (200 mL, 200 mmol) over 90 minutes. The cooling bath was removed and the reaction mixture was stirred at room temperature for two days. The remaining borane was quenched by the slow addition of saturated sodium bisulfate (10 mL) over 90 min with cooling. Additional saturated sodium bisulfate (200 mL) was added and after 20 min of stirring the aqueous layer was removed. The organic layer was washed with water and saturated sodium chloride, dried, filtered and concentrated. The residue was purified by flash chromatography using 20% diethylether in hexanes to give 1-methyl-1-hydroxymethylcyclohexane (6.17 g, 48 mmol, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244721B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-16f50c8e17174c7382e204117cb0c28c |
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| Source note | uspto-grants-2007_07 |
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