HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635398Generated: October 25, 2026
Potassium Cyanide → 3-Cyano-5-nitrobenzoic acid
https://huagongshe.com/reaction/635398
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Amino-5-nitrobenzoic acid | HCID 239342 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Cyano-5-nitrobenzoic acid | HCID 21942565 | 94% |
Reaction Steps
3-Amino-5-nitrobenzoic acid (3.64 g, 20 mM) was dissolved in concentrated hydrochloric acid (20 ml), diluted with water (75 ml), cooled to 0°, and added over 30 minutes to a solution of NANO2 (1.38g, 20 mM) in water (10 ml). The pH was adjusted to 6.2 with saturated Na2CO3 solution. A mixture of CuSO4.5H2O (10 g, 42 mM) in water (40 ml) and KCN (10 g, 154 mM) in water (20 ml) was heated to 65°, the solution of diazonium salt added over 15 minutes, and the mixture refluxed for 40 minutes. After cooling, and acidifying with 2M hydrochloric acid, the organics were extracted into ethyl acetate (2×200 ml). The combined extracts were washed with aqueous NaH2PO4, water, brine, and dried over Na2SO4. Evaporation gave 3-cyano-5-nitrobenzoic acid (3.6 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187804B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-40e536382091473ea72c997782e673e9 |
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| Source note | uspto-grants-2001_02 |
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