HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylethyl 2-methoxyacetate → Methyl (1S,2S)-2-aminocyclohexane-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylethyl 2-methoxyacetate | HCID 542192 | — |
| Reactant | Methyl (1R,2R)-2-aminocyclohexane-1-carboxylate | HCID 11768827 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Methyl (1S,2S)-2-aminocyclohexane-1-carboxylate | HCID 10964775 | 46.7% |
Reaction Steps
50 g (0.32 mol) of methyl trans-2-aminocyclohexanecarboxylate were dissolved in 200 ml of MTBE and, after addition of 0.16 mol of isopropyl methoxyacetate and 0.5 g of Novozym 435 (Novo Nordisk), shaken at room temperature for 8 h. The enzyme was filtered off and then the solvent was removed and the residue was distilled under reduced pressure. 23.5 g of methyl (1S,2S)-2-aminocyclohexanecarboxylate and 35.2 g of methyl (1R,2R)-2-(2-methoxyacetylamino) cyclohexanecarboxylate were obtained, each with an ee of 99.8%. The ee of the amine was determined after N-acylation with acetic anhydride by gas chromatography on a B-PH GC column (supplied by Astec, N.J., USA), while the N-2-methoxyacetamide was put on this column without derivatization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06063615 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-d5754a2c731c4a1ab2b3cc74f5e8a928 |
| Source note | uspto-grants-2000_05 |