Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Cis tert-Butyl 4-aminocyclohexylcarbamate | HCID 2756050 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66955715 | HCID 66955715 | 112.9% |
Reaction Steps
Methyl chloroformate (0.468 mL, 6.06 mmol) was added dropwise, over a period of 20 min, under argon atmosphere, at 0° C., to a mixture of (4-amino-cyclohexyl)-carbamic acid tert-butyl ester (1.0 g, 4.67 mmol) and pyridine (0.479 mL, 6.06 mmol) in THF (6 mL) and the resulting mixture was stirred at RT for 24 h. The reaction mixture was then evaporated under reduced pressure and water (300 mL) was added to the solid residue. The resulting mixture was extracted 3 times with EtOAc (100 mL), the combined organics were washed 3 times with water (100 mL), twice with NaHSO4 (aq 1%, 150 mL) and twice with water (150 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The remaining white solid was mixed with HCl (2.0 M in MeOH, 200 mL) and the resulting mixture was stirred at RT for 5 h. The reaction mixture was then evaporated under reduced pressure to give 1.1 g of (4-amino-cyclohexyl)-carbamic acid methyl ester hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268840B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-2e543b7f386540208b7aff2f6e2a9741 |
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| Source note | uspto-grants-2012_09 |
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