HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900146Generated: October 29, 2026
Hydrochloric Acid → HCID 178424372, compound
https://huagongshe.com/reaction/1900146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178424371 | HCID 178424371 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178424372 | HCID 178424372 | — |
Reaction Steps
N-(2-Methylphenyl)-N'-(2-methyl-4-aminophenyl)guanidine dihydrochloride (112 mg, 0.341 mmol) were dissolved in 2 ml H2O and 100 ul cone. HCl (1.2 mmol). The solution was cooled in an ice bath, and a solution of NaNO2 (42 mg, 0.61 mmol) in 450 ul H2O were added. The reaction mixture turned yellow, and was stirred for 45 min before solid NaN3 (43 mg, 0.661 mmol) was added in a single portion. After N2 evolution was caused, a foamy solid (11 mg) was removed and discarded. Solid NaOH (96 mg, 2.41 mmol) was added, and the bright yellow precipitate was extracted with Et2O (3×5 ml). Evaporation of the combined Et2O layers gave a yellow solid which was crystallized from EtOH/H2O: NMR (CD3OD) δ2.279 (s, 3H), 2.284 (s, 3H), 6.864 (dd, 1H, J=2.4 Hz, 8.4 Hz), 6.914 (d, 1H, J=2.1 Hz), 7.055 (td, 1H, J=1.8 Hz, 7.2 Hz), 7.136-7.229 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574070 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-44487399da7842a5a7a36c8404f15a80 |
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| Source note | uspto-grants-1996_11 |
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