HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389374Generated: October 31, 2026
Hydrochloric Acid → [2-(3-Methoxybenzyl)cyclohexyl]methanol
https://huagongshe.com/reaction/2389374
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 19358413 | HCID 19358413 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(3-Methoxybenzyl)cyclohexyl]methanol | HCID 68533760 | 80.2% |
Reaction Steps
Under N2 gas atmosphere, to a stirred mixture of lithium aluminum hydride (0.703 g) in THF (9 mL) was added 2-(3-methoxybenzyl)cyclohexanecarboxylic acid (2.3 g) in THF (9 mL) dropwise at 0° C. The reaction mixture was stirred at 0° C. for an hour, at ambient temperature for an hour, at 60° C. for 4 hours. The reaction mixture was cooled to 0° C. and was added mixed solution (1M HCl aqueous solution:THF=10:90) dropwise. The resulting mixture was diluted with water and was extracted with diethylether two times. The organic layer was dried over anhydrous MgSO4, filtered and evaporated in vacuo. The mixture was purified by thin-layer chromatography (n-hexane:EtOAc=5:1) to give [2-(3-methoxybenzyl)cyclohexyl]methanol (1.74 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273745B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-399a25e4469b4631bbdec8bb02b95d6c |
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| Source note | uspto-grants-2012_09 |
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