Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 62358690 | HCID 62358690 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 20431-81-6 | HCID 316731 | 84% |
Reaction Steps
To a solution of (2-hydroxy-cyclohexyl)-carbamic acid ethyl ester (2.06 g, 11.0 mmol, 1.0 eq.) in THF (80 mL) was added LiAlH4 (1.09 g, 28.7 mmol, 2.6 eq.) and the resulting mixture was heated at 65° C. for 2 h. The reaction mixture was cooled to 0° C., quenched with water, and the separated aqueous phase was extracted with 3×EtOAc. The combined organic phase was dried over MgSO4, filtered and concentrated to give 2-methylamino-cyclohexanol (1.19 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314936B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-2b4ded9e44f84b38b6e9b9ed0c79ab5a |
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| Source note | uspto-grants-2008_01 |
|---|