HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → HCID 58109706, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 58109514 | HCID 58109514 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58109706 | HCID 58109706 | 280.7% |
Reaction Steps
To the solution of 3-(3-bromophenylamino)-1-phenylpropan-1-one (0.03 mol) in anhydrous THF (30 mL) was added K2CO3 (0.06 mol) and methyl chloroformate (0.033 mol) at 0° C. under N2 atmosphere. Then the reaction mixture was stirred at rt for 2 h. The resulting mixture was filtered and the filtrate was concentrated. The residue was washed with H2O, 1N HCl and brine and then extracted with EtOAc. The combined organic layers were concentrated to give crude product, which was purified by column chromatography to afford methyl 3-bromophenyl(3-oxo-3-phenylpropyl)carbamate (30.5 g, 95%). 1H NMR (400 MHz, CDCl3): δ=3.22 (m, 2H), 3.62 (s, 3H), 4.02 (m, 2H), 7.05-7.20 (m, 2H), 7.3-7.5 (m, 4H), 7.8 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575156B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-ad11d38cdcba417fa186fad7dbf47dfd |
| Source note | uspto-grants-2013_11 |