HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → (2-Acetyl-cyclohexyl)-carbamic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Ethyl (1R,2S)-2-aminocyclohexane-1-carboxylate hydrobromide | HCID 122236269 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Acetyl-cyclohexyl)-carbamic acid benzyl ester | HCID 20732580 | 98% |
Reaction Steps
To a 0° C. solution of ethyl cis-2-amino-1-cyclohexanecarboxylate HBr salt (22.34 g, 88.6 mmol) in 250 mL of methylene chloride, was added benzyl chloroformate (12.6 mL, 88.3 mmol) and 250 mL of an aqueous sodium carbonate solution. The reaction mixture was stirred for 24 h at ambient temperature. The organic layer was separated and washed with 250 mL of water, dried over sodium sulfate, filtered and concentrated to give a crude liquid. The product was purified by column chromatography (10-50:90-50 ethyl acetate/hexanes) to give 26.45 g of (2-acetyl-cyclohexyl)-carbamic acid benzyl ester as a clear liquid. Yield: 98%, MS: 306 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07300934B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-2ff250ba1c11443fb3c0cf81a0f0bb1e |
| Source note | uspto-grants-2007_11 |