HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminocyclohex-1-ene-1-carbonitrile → 2-aminocyclohexane-1-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminocyclohex-1-ene-1-carbonitrile | HCID 290175 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-aminocyclohexane-1-carbonitrile | HCID 21163863 | 78.6% |
Reaction Steps
To a cold solution of 2-aminocyclohex-1-enecarbonitrile (I-7a: 50 mg, 0.41 mmol) in methanol (3 mL) was added NaCNBH3 (103 mg, 1.64 mmol) and acetic acid (5 drops) at 0° C. The resulting mixture was stirred at room temperature for 16h. The reaction mixture was diluted with ethyl acetate and the organic layer was washed with saturated NaHCO3, brine, dried over anhydrous Na2SO4 and concentrated to afford 40 mg (78%) of diastereomeric mixture of 2-aminocyclohexanecarbonitrile (I-7b) as a gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447039B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-362529fe20684a55b771015a2944a1df |
| Source note | uspto-grants-2016_09 |