Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(2,4-Dinitroanilino)benzoic acid | HCID 627514 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21704275 | HCID 21704275 | 67.1% |
Reaction Steps
1.80 g (6 mmol) of 2-(2,4-dinitrophenylamino) benzoic acid, 2.66 g (42.6 mmol) of ammonium chloride, 2.4 ml of ammonia, concentrated, 52 ml of ethanol, and 21 ml of distilled water are combined at an internal temperature of 78° C. (bath temperature 90° C.). To this batch is added, in 3 portions, 4.44 g (20 mmol) of sodium sulfide (35% strength) and the mixture is stirred for one hour. The batch is suctioned off at room temperature and washed in succession with water and ether. The filtrate is concentrated to the aqueous phase and extracted by shaking with ethyl acetate. The organic phase is dried, filtered, and concentrated. The aqueous phase is acidified with 1N hydrochloric acid and suctioned off, thus obtaining 1.1 g of 2-(2-amino-4-nitrophenylamino)benzoic acid (processed without purification).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057304 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-c35494331f674ded8d50704645d93ab7 |
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| Source note | uspto-grants-2000_05 |
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