HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781036Generated: October 31, 2026
4-Methyl-2,6-dinitroaniline → HCID 10487280, compound
https://huagongshe.com/reaction/1781036
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methyl-2,6-dinitroaniline | HCID 22892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10487280 | HCID 10487280 | 85% |
Reaction Steps
The procedure of Gillespie et al., J. Org. Chem. 25:942 (1960) was adopted as follows. A dark black solution of 4-methyl-2,6-dinitroaniline (0.100 g, 0.561 mmol, Aldrich, used as received) in 6.66% aq. (NH4)2S (3.3 mL, prepared from 20% aq.(NH4)2S solution supplied by Aldrich) and ethanol (3.5 mL) was refluxed for 45 min. It was then cooled to 28° C. and the solvents were removed as much as possible under vacuum (inside the hood to avoid the stench of ammonium sulfide). The slurry so obtained was diluted with water (10 mL) and the resulting red solid was filtered and dried under vacuum to obtain 0.072 g (85%) solid as a red powder, which was used as such for the next reaction. 1H NMR (acetone-d6): 2.205 (s, 3H), 6.342 (br s, 2H), 6.622 (s, 1H), 7.571 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05631373 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-cb4d580f1a1646c0b4045ba962cee035 |
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| Source note | uspto-grants-1997_05 |
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