Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 5-Amino-2,4,6-tribromo-1,3-benzenedicarboxylic acid | HCID 18432427 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 20443396 | HCID 20443396 | 55% |
Reaction Steps
2,4,6-Tribromo-5-amino-isophthalic acid (232 g; 0.555 mole) is dissolved in concentrated sulfuric acid (500 ml) and the solution is then cooled by means of an ice-bath to a temperature between 0° and 5° C. Sodium nitrite (77 g; 1.11 mole) is then added portionwise over 1 hour while maintaining the temperature at 0°-5° C., and the mixture is stirred for a further 2 hours at that temperature. The mixture is then slowly poured over ice, with stirring, and the excess sodium nitrite is destroyed with a sufficient amount of urea solution. While still maintaining the temperature at 0°-5° C., the suspension is neutralized at pH 6 by addition of 5N sodium hydroxide. The mixture is then added to a solution of cuprous chloride (69 g; 0.694 mole) and sodium cyanide (89 g; 1.82 mole) in 1 liter water, and the solution is stirred overnight at room temperature. The pH of the solution is adjusted to 3 by addition of hydrochloric acid, the copper salt precipitate is suction filtered, and the pH is adjusted to 1 with hydrochloric acid. The solution is cooled in an ice-bath and stirring is maintained for a further 16 hours. The resulting precipitate is suction filtered; it is then taken up into 400 ml water, with stirring, plus a sufficient amount of sodium hydroxide for dissolution and neutral pH. The solution is decolorized by stirring for 1 hour with charcoal 3 SA, after which the charcoal is filtered off, and the material is precipitated with dilute hydrochloric acid to give, after suction filtering and washing with a small amount of water, 130 g of white product (Yield: 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04474747 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-3128f76a88d94ce9a8c857a74168dd72 |
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| Source note | uspto-grants-1984_10 |
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