HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730619Generated: October 25, 2026
Hydrochloric Acid → 1,2-Benzenedicarbonitrile, 4-nitro-
https://huagongshe.com/reaction/1730619
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1,2-Benzenedicarboxamide, 4-nitro- | HCID 83167 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1,2-Benzenedicarbonitrile, 4-nitro- | HCID 97443 | 50.1% |
Reaction Steps
4-nitrophthalamide (220 g; 1.05 moles) is suspended in pyridine (840 ml). Into this vigorously stirred suspension, phosphorus oxychloride (220 ml; 2.40 moles) is added at such a rate that the reaction maintains a temperature range of 65°-70° C during the 30-minute addition time. The same temperature is maintained an additional hour by external heating. The resulting mixture is neutralized with 12 N hydrochloric acid (150 ml). The purple solid is collected by filtration and dried. The residue is extracted with ethyl acetate (3 × 700 ml) and the purple extract is decolorized with activated charcoal, washed first with 0.4N sodium hydroxide saturated with sodium chloride (3 × 70 ml) and then with water (4 × 70 ml). Drying and evaporation of the extract leaves 91 g of II as pale yellow crystals; yield, 50%; mp 142-144°; lit. (7-mp 138°-139°; lit. (4) 142°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03993631 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-640035ed37c44aee8664d8f25591f018 |
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| Source note | uspto-grants-1976_11 |
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