HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334028Generated: October 29, 2026
Acetic Acid → 2H-Tetrazole-5-carboxylic acid, 2-(3-chlorophenyl)-, ethyl ester
https://huagongshe.com/reaction/334028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | N'-(3-chlorophenyl)-2-ethoxyacetohydrazonamide | HCID 86688257 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2H-Tetrazole-5-carboxylic acid, 2-(3-chlorophenyl)-, ethyl ester | HCID 574534 | — |
Reaction Steps
12.0 mL (210 mmol) acetic acid was added to a solution of 12.0 g (52.7 mmol) N′-(3-chloro-phenyl)-2-ethoxyacetohydrazonamide in 120 mL THF. The mixture was heated to 85° C. and a solution of 4.36 g (63.2 mmol) sodium nitrite in 12 mL water was added over 4 h. After stirring for 1 h at 85° C., the mixture was cooled to RT. The solvent was evaporated. The residue was dissolved in EtOAc and extracted with aqueous sodium bicarbonate. The organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated. The resulting residue was purified by column chromatography eluted with hexane/EtOAc (90:10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883789B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-76622975f6764fc3953b86e7eaf3c459 |
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| Source note | uspto-grants-2014_11 |
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