Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 590558 | HCID 590558 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13341946 | HCID 13341946 | — |
Reaction Steps
3,4-Dihydro-2-trichloromethyl-2H-benzo[e]-[1,3]-oxazin-4-one (prepared as described in Example 3--5 g.) was suspended in ethanol (100 ml.), 63 ml. of a solution of sodium hydroxide (1.0 g.) in ethanol (83 ml.) was added, and the mixture was stirred for 15 minutes to obtain a clear solution. Iodomethane (5 ml.) was added, and the solution was boiled under reflux for 30 minutes. The solvents were evaporated, and the residue was dissolved in a mixture of toluene and ethyl acetate (7:3 by volume) and chromatographed on silica, eluting with the same solvent mixture. The first 100 ml. of eluate was collected, the solvent was evaporated and the residue crystallised on trituration with petroleum ether (b.p. 60°-80° C.) to give 3,4-dihydro-3-methyl-2-trichloromethylbenzo[e]-[1,3]-oxazin-4-one, m.p. 82°-84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04268510 |
|---|
| Source dataset | uspto-grants-1981_05 |
|---|
| ORD ID | ord-03e189e7be6f4b1b90e2c46c3619fd75 |
|---|
| Source note | uspto-grants-1981_05 |
|---|