Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 13608182 | HCID 13608182 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21243220 | HCID 21243220 | 82.8% |
Reaction Steps
To a solution of 3,4-dihydro-6-(4-methoxy-3-methylthiophenyl)-1,3-dimethyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinone (1.5 g) in N,N-dimethylformamide (15 ml) was added m-chloroperbenzoic acid (1.58 g), and stirred at 5°-10° C. for 30 minutes, and at ambient temperature for 5 hours. To the reaction mixture was added water (50 ml), and extracted with ethyl acetate. The organic layer was washed with aqueous sodium bicarbonate solution, dried over sodium sulfate, and evaporated. The residue was chromatographed on silica gel, eluting with chloroform. The fractions containing a sulfonyl compound were collected, dissolved in 1-N-hydrochloric acid and neutralized by aqueous sodium bicarbonate solution to give powdery 3,4-dihydro-6-(4- ro methoxy-3-methylsulfonylphenyl)-1,3-dimethyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinone (0.78 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04649142 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-098f371fab434de4b0439d61c52c1830 |
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| Source note | uspto-grants-1987_03 |
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