HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → Methyl 2-amino-5,5-dimethylcyclohex-1-enecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Methyl 2-hydroxy-5,5-dimethylcyclohex-1-enecarboxylate | HCID 54676124 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 2-amino-5,5-dimethylcyclohex-1-enecarboxylate | HCID 66820389 | 75% |
Reaction Steps
A solution of methyl 2-hydroxy-5,5-dimethylcyclohex-1-enecarboxylate (10.0 g, 54 mmol) and ammonium acetate (10 g, 130 mmol) in ethanol (50 mL) was heated to reflux for 2 hours. The reaction was concentrated to one third original volume, and then diluted with ethyl acetate (100 mL). The organic solution was washed with water (100 mL) and brine (50 mL) and then dried over anhydrous sodium sulfate. After filtration and concentration, the residue was purified by silica gel column chromatography (ethyl acetate/hexanes, 1:8) to afford methyl 2-amino-5,5-dimethylcyclohex-1-enecarboxylate (7.42 g, 75% yield) as a yellow solid. MS (EI) for C10H17NO2: 184 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648066B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-480ddb7ec6be479e9bf452fc258b24b4 |
| Source note | uspto-grants-2014_02 |