HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848057Generated: November 1, 2026
Sodium Hydroxide → (1-(Aminomethyl)cyclohexyl)methanol
https://huagongshe.com/reaction/1848057
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Methyl 1-cyanocyclohexane-1-carboxylate | HCID 11182833 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-(Aminomethyl)cyclohexyl)methanol | HCID 22379486 | 58.4% |
Reaction Steps
To a stirred solution of methyl 1-cyanocyclohexanecarboxylate (2 g, 11.96 mmol) in anhydrous THF (40 mL) at rt was added portionwise LiAlH4 (1.36 g, 35.88 mmol). The reaction vessel was sealed and the mixture was heated at 80° C. for 5 h. The mixture was cooled to 0° C. and water (1 mL), 1M aq NaOH (1 mL), and water (3 mL) were added sequentially. To the resulting mixture were added DCM and saturated aq sodium potassium tartrate, and the mixture was stirred for 3 h. The organic layer was separated and further washed with brine. The organic layer was separated, dried over MgSO4, filtered, and concentrated under reduced pressure to afford (1-(aminomethyl)cyclohexyl)methanol (1 g) which was not purified further. LCMS (ESI) m/z 144 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952058B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-40ab976a1e3a4bc590e572b67738b5a9 |
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| Source note | uspto-grants-2015_02 |
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