HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → cis-Methyl 3-acetamidocyclohexanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Methyl (1S,3R)-3-aminocyclohexane-1-carboxylate | HCID 68466059 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | cis-Methyl 3-acetamidocyclohexanecarboxylate | HCID 131730829 | 69.2% |
Reaction Steps
Acetic anhydride (1.20 ml, 12.7 mmol) was added to a stirred solution of cis-methyl 3-aminocyclohexanecarboxylate (0.40 g, 2.54 mmol) in pyridine (10 ml) under an atmosphere of argon and stirred for 3 h at room temperature. The excess pyridine was removed under vacuo and the resulting residue was partitioned between DCM and saturated sodium bicarbonate solution. The separated organic layer was washed with water, brine, dried over anhydrous sodium sulfate, filtered and concentrated under vacuo to afford cis-methyl 3-acetamidocyclohexanecarboxylate (350 mg, 69.0%) as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067888B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-8aaa3d894a524892b3e55f92373b0d03 |
| Source note | uspto-grants-2015_06 |