HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216246Generated: October 31, 2026
HCID 21941239, compound → HCID 178499399, compound
https://huagongshe.com/reaction/2216246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21941239 | HCID 21941239 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178499399 | HCID 178499399 | 71.5% |
Reaction Steps
Methyl 4-acetamido-3-aminophenylacetate (77 g, 0.373 mol) was taken up in a mixture of acetic acid (210 ml) and water (210 ml) and cooled to below 5° C. A solution of sodium nitrite (38.63 g, 0.559 mol) in water (200 ml) was added dropwise, and once the addition was complete the mixture was stirred for 4 hours, warming slowly to room temperature. The mixture was diluted with ethyl acetate and the insoluble material removed by filtration. The filtrate was washed with brine, dried over anhydrous magnesium sulfate, filtered and the solvent evaporated in vacuo, to give a viscous residue (51 g) which was then dissolved in a solution of methanol (400 ml) previously saturated with hydrogen chloride and the mixture stirred for 2 hours. The solvent was removed in vacuo, the residue taken up in water, neutralised with saturated aqueous sodium bicarbonate solution and extracted with ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated in vacuo to afford methyl 5-benzotriazoleacetate (35 g) as a reddish liquid which crystallised on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112553B1 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-8dd2751e43434c598fe285bc37c9a020 |
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| Source note | uspto-grants-2006_09 |
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