Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzoyl chloride, 3-nitro- | HCID 8495 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,7-Naphthalenedisulfonic acid, 3-amino-5-hydroxy- | HCID 66658 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Disodium | HCID 141233 | — |
| Product | HCID 20496770 | HCID 20496770 | — |
Reaction Steps
A 41.0 g portion of recrystallized 3-amino-5-hydroxy-2,7-naphthalenedisulfonic acid and 16.5 g of sodium acetate trihydrate are dissolved in 250 ml of distilled water, then 44.55 g of m-nitrobenzoyl chloride is added all at once along with 120 ml of 1 N sodium hydroxide and a small amount of diethyl ether. The resulting mixture is shaken for 5 minutes, another 120 ml of 1 N sodium hydroxide and a small amount of diethyl ether. The resulting mixture is shaken for 5 minutes, another 120 ml of 1 N sodium hydroxide is added and the mixture is shaken for 1/2 hour. The latter addition and shaking is repeated two more times. The resulting mixture is acidified to Congo Red indicator paper with concentrated hydrochloric acid and allowed to stand at 5° C. for 17 hours. The solution is filtered and the filtrate allowed to stand until a precipitate forms. The precipitate is stirred with about 400 ml of diethyl ether and collected to give 5-hydroxy-3-m-nitrobenzamido-2,7-naphthalenedisulfonic acid, disodium salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04391824 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-b8dec2aa45d946f1af0bfc63cf6aec12 |
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| Source note | uspto-grants-1983_07 |
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