HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → methyl N-[1-(3-bromophenyl)ethyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 1-(3-Bromophenyl)ethanamine | HCID 16785764 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | methyl N-[1-(3-bromophenyl)ethyl]carbamate | HCID 15483792 | 34.2% |
Reaction Steps
To a solution of 23.8 g of 3-bromo-α-methylbenzylamine in toluene (120 ml), 14.1 g of pyridine was added at room temperature. To this solution, 18.6 g of methyl chloroformate was dropwise added under cooling with ice, followed by stirring at room temperature for 2 hours. The reaction solution was poured into a citric acid aqueous solution and extracted with ethyl acetate. The organic layer was washed with a citric acid aqueous solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 10.5 g of methyl N-[1-(3-bromophenyl)ethyl]carbamate as a colorless transparent viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313071B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-f9f3808b31a5484d9c9deeeb7c97155d |
| Source note | uspto-grants-2001_11 |