HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-6-phenyl-3-m-tolyl-1,3-oxazinan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | (S)-3-(m-tolylamino)-1-phenylpropan-1-ol | HCID 58200036 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-6-phenyl-3-m-tolyl-1,3-oxazinan-2-one | HCID 44231030 | 67% |
Reaction Steps
To a solution of (S)-3-(m-tolylamino)-1-phenylpropan-1-ol (40 mg, 0.17 mmol) in dry CH2Cl2 (1 mL) was added triethylamine (50 mg, 0.51 mmol) and bis(trichloromethyl) carbonate (20 mg, 0.067 mmol) at 0° C., and the reaction mixture was stirred overnight at room temperature. When the reaction was over, the mixture was concentrated to give the crude product, which was purified by preparative TLC (3:1 Petroleum ether/EtOAc) to give (S)-6-phenyl-3-m-tolyl-1,3-oxazinan-2-one (12 mg, 26%). 1H NMR: (400 MHz, CDCl3): δ=2.24-2.37 (m, 5H), 3.52-3.63 (m, 1H), 3.70-3.79 (m, 1H), 5.42 (dd, 1H), 7.01-7.10 (m, 3H), 7.18-7.23 (m, 2H), 7.32-7.39 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598160B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-e414678c489c4bfe882e487173b3bdf6 |
| Source note | uspto-grants-2013_12 |