HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-{[(Benzyloxy)carbonyl]amino}-3-(1-methylcyclohexyl)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2-(benzyloxycarbonylamino)-3-(1-methylcyclohexyl)propanoate | HCID 59201682 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-{[(Benzyloxy)carbonyl]amino}-3-(1-methylcyclohexyl)propanoic acid | HCID 59201721 | 36% |
Reaction Steps
A mixture of methyl 2-(benzyloxycarbonylamino)-3-(1-methylcyclohexyl)propanoate, 10.00 g of KOH, 100 mL of MeOH, and 20 mL of water was vigorously stirred at rt for 17 h. After methanol was evaporated under reduced pressure, the residue was diluted with water and extracted with Et2O (2×). The aqueous phase was treated with 100 mL of 2 NHCl, extracted with EtOAc (3×), and dried over Na2SO4. The extracts were evaporated under reduced pressure to afford 1.5150 g (36% in two steps) of 2-(benzyloxycarbonylamino)-3-(1-methylcyclohexyl)propanoic acid. MS ESI +ve m/z 320 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08487108B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-0b45424b9fb34b919301478106d6887d |
| Source note | uspto-grants-2013_07 |