Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 19735140 | HCID 19735140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19735134 | HCID 19735134 | — |
Reaction Steps
m-Chloroperbenzoic acid (70% purity, 4.64 g) was added with ice-cooling to a solution of 2,2-dimethyl-6-phenylthio-3,4-dihydro-2H-1,3-benzoxazin-4-one (2.24 g) in dichloromethane (50 ml) and the mixture was stirred for 30 minutes. The reaction mixture was poured into an aqueous sodium sulfite solution and the mixture was extracted by addition of ethyl acetate. The organic layer was successively washed with an aqueous sodium carbonate solution and saturated saline solution, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was washed with isopropyl ether to obtain 2,2-dimethyl-6-phenylsulfonyl-3,4-dihydro-2H-1,3-benzoxazin-4-one (2.50 g) (Compound A-13). The physical properties are shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05270308 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-39b3fd8352d24bc79e286f9105fc44b5 |
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| Source note | uspto-grants-1993_12 |
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