HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Aminocyclohexanecarboxylic acid → Methyl 1-aminocyclohexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Aminocyclohexanecarboxylic acid | HCID 1366 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Product | Methyl 1-aminocyclohexanoate | HCID 4048819 | 52% |
Reaction Steps
To a solution of 1-aminocyclohexanecarboxylic acid (600 mg) in tetrahydrofuran-methanol was added dropwise trimethylsilyl diazomethane (4.2 mL) under ice-cooling and stirring, and the mixture was stirred overnight. The reaction mixture was concentrated in vacuo, and to the residue were added successively diethylether-hexane (1/1) and a solution of 4N hydrochloric acid in ethyl acetate (1.05 mL). The precipitates were collected by filtration and dried to give methyl 1-amino-cyclohexanecarboxylate (423 mg, yield: 52%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163759B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-4326a4f70dbc48ed99da68ff86de5218 |
| Source note | uspto-grants-2012_04 |