HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Nitro-4-(phenylmethanesulfinyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-[2-Nitro-4-(phenylmethanesulfinyl)phenyl]acetamide | HCID 20362831 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Nitro-4-(phenylmethanesulfinyl)aniline | HCID 21328043 | — |
Reaction Steps
2.42 G. 1-acetamido-2-nitro-4-benzylthiobenzene in 25 ml. chloroform is treated at -20 to -15° C with 1.6 g. 40% peracetic acid in 2 ml. methanol. The mixture is allowed to warm slowly to room temperature, held for 6 hours and washed with sodium bisulfite solution and sodium bicarbonate solution, dried and stripped. The residue is recrystallized from methanol giving 1-acetamido-2-nitro-4-benzylsulfinylbenzene. 2.14 G. 1-acetamido-2-nitro-4-benzylsulfinylbenzene is treated with 4 ml. 5N sodium hydroxide and 12 ml. methanol, on steam bath for 30 minutes, diluted with water, and filtered to give 1-amino-2-nitro-4-benzylsulfinylbenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002640 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-fe1a314942ec44d4b9ea56b8fe95b845 |
| Source note | uspto-grants-1977_01 |