HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256348Generated: October 29, 2026
Hydrochloric Acid → HCID 178513866, compound
https://huagongshe.com/reaction/256348
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 13682654 | HCID 13682654 | — |
| Reactant | HCID 178509300 | HCID 178509300 | — |
| Product | HCID 178513866 | HCID 178513866 | 43% |
Reaction Steps
A mixture of 5.0 g (0.023 mole) of 3,6-dimethoxy-2-benzofurancarboxylic acid and 8.0 g (0.049 mole) of 1,1-carbonylbis(1H-imidazole) in 60 ml of N,N-dimethylformamide is stirred and warmed on the steam bath for 20 minutes. The mixture is cooled to room temperature, 2.5 g (0.024 mole) of 5-aminotetrazole monohydrate is added, and the new mixture is again heated for 20 minutes. The reaction mixture is cooled, added to 350 g of ice/water and acidified with 4.0 N hydrochloric acid to precipitate the tetrazole product. The precipitate is filtered, washed with 50% aqueous ethanol, and recrystallized from aqueous N,N-dimethylformamide to yield 2.8 g (43% yield) of the analytically pure 3,6-dimethoxy-N- 1Htetrazol-5-yl-2-benzofurancarboxamide, mp 238° C.-dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04703053 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-21f5290a192a423eb8a86eefe54a444b |
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| Source note | uspto-grants-1987_10 |
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