HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → (+/-)-(1S,2S)-2-amino-1-methylcyclohexanolhydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | (+/-)-benzyl (1S,2S)-2-hydroxy-2-methylcyclohexylcarbamate | HCID 86707706 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (+/-)-(1S,2S)-2-amino-1-methylcyclohexanolhydrobromide | HCID 86707707 | — |
Reaction Steps
To (±)-Benzyl (1S,2S)-2-hydroxy-2-methylcyclohexylcarbamate (81.4 mg, 0.309 mmol) was added HBr in AcOH, 33% (1 mL, 6.1 mmol) and the resulting mixture was stirred at rt under N2 for 2 h. The solvents were removed and the crude residue concentrated with EtOH (2×) and dried on high vacuum overnight to afford an orange low-melting solid which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921368B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-7eaf93c4e5f042c0b3f0639cad8a2d94 |
| Source note | uspto-grants-2014_12 |