HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323450Generated: October 30, 2026
1,2-Hydrazinedicarboxaldehyde → methyl 2-methoxy-5-(4H-triazol-1-yl)benzoate
https://huagongshe.com/reaction/323450
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Hydrazinedicarboxaldehyde | HCID 12342 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | Methyl 5-amino-o-anisate | HCID 89843 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Dichloromethane ethylacetate | HCID 21226138 | — |
| Product | methyl 2-methoxy-5-(4H-triazol-1-yl)benzoate | HCID 22009369 | — |
Reaction Steps
Alternately, according to the method of J. Med. Chem., 21, 1100 (1978), combine methyl 2-methoxy-5-aminobenzoate (1.8 g, 10 mmol), diformyl hydrazine (0.97 g, 11 mmol), and phosphorous pentoxide (1.84 g, 13 mmol). Heat to 160° C. After 1.5 hours, cool the reaction mixture and add a saturated aqueous solution of sodium bicarbonate. Extract three times with dichloromethane. Dry the combined organic layers over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 40% ethyl acetate/dichloromethane and then 5% methanol/dichloromethane to give methyl 2-methoxy-5-(4H-triazol-1-yl)benzoate: mp; 179-182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211199B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-51d4e5ada01148b294c4f63a0dbc22fa |
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| Source note | uspto-grants-2001_04 |
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