Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | N-{2-Nitro-4-[(prop-2-en-1-yl)sulfanyl]phenyl}acetamide | HCID 14273283 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20371014 | HCID 20371014 | — |
Reaction Steps
3.0 G. of 1-acetamido-2-nitro-4-(prop-2-en-1-yl-thio)benzene, prepared according to Example I, in 30 ml. chloroform is cooled to -15° C. and treated with a solution of 2.5 g. of 40% peracetic acid in 4 ml. methanol. After the addition, the temperature is allowed to rise slowly to 20° C whereupon the solution is washed with sodium bisulfite solution and then with sodium bicarbonate solution. The product is isolated by evaporation of the solvent and purified to afford 1-acetamido-2-nitro-4-(prop-2-en-1-ylsulfinyl)benzene. This is treated with 20 ml. methanol and 10 ml. 5N aqueous sodium hydroxide at 20°-25° C. for one hour. The mixture is diluted with water and the crude product filtered off. Recrystallization yields 1-amino-2-nitro-4-(prop-2-en-1-ylsulfinyl)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04072696 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-c1b923daaf6e4fdaa4458f08f6fad051 |
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| Source note | uspto-grants-1978_02 |
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