Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,6-Dinitrophenol | HCID 11312 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium sulfide nonahydrate | HCID 73972 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-6-nitrophenol | HCID 5127291 | 68.3% |
Reaction Steps
A suspension of 2,6-dinitrophenol (5 g), ammonia (3 ml) and ammonium chloride (14.30 g) in water (30 ml) was heated to 70° C. A solution of sodium sulphide nonahydrate (24.19 g) in water (23 ml) was added and the resulting mixture stirred at 70° C. for 2 hours. The reaction was cooled to room temperature, acidified (pH 3.2) with 2N HCl, and the brown precipitate separated by filtration. The filtrate was extracted with chloroform (6×75 ml), the organic extracts combined with the precipitate, and evaporated in-vacuo to yield a dark brown solid. The solid was purified by flash chromatography (SiO2; dichloromethane) to yield the title compound (2.86 g, 68%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06372770B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-95f6ea7ffb254dc899a0187a069e42c5 |
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| Source note | uspto-grants-2002_04 |
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