HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621850Generated: October 25, 2026
4-Chlorobenzoic Acid → HCID 178477971, compound
https://huagongshe.com/reaction/621850
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzoic Acid | HCID 6318 | — |
| Reactant | 2,3-Diaminopyridine | HCID 9956 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 178477971 | HCID 178477971 | 4.4% |
Reaction Steps
A mixture of 2,3-diaminopyridine (10.9 g, 0.1 mole), p-chlorobenzoic acid (16.0 g, 0.102 mole), and 150 g of polyphosphoric acid was heated at 180° C. in an oil bath for 31/2 hr. The reaction mixture was neutralized with concentrated ammonium hydroxide and basified with sodium hydroxide. The precipitate was filtered and washed with water. The solid was treated with dilute sodium hydroxide, filtered, washed with water, and dried under high vacuum at 60° C. overnight. A 3-g sample was dissolved in hot methanol, and the solution was treated with 3 g of charcoal, and filtered through a Celite pad. The product crystallized from the filtrate upon cooling. The precipitate was filtered, washed with methanol-water (2:1), and dried under high vacuum at 70° C. to give 1.0 g of the title compound, mp 305°-8° C. with sublimation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04824951 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-049ebbbfdad54b5e970b0bfd4b8f922b |
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| Source note | uspto-grants-1989_04 |
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