HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13961715, compound → HCID 178493575, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13961715 | HCID 13961715 | — |
| Reactant | HCID 178509299 | HCID 178509299 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178493575 | HCID 178493575 | — |
Reaction Steps
A mixture of 0.90 g (0.0034 mole) of 3-methoxy-5-phenyl-2-benzofurancarboxylic acid and 0.55 g (0.0034 mole) of 1,1-carbonylbis(1H-imidazole) in 25 ml of tetrahydrofuran is stirred at reflux for one hour. To the mixture is added 0.29 g (0.0034 mole) of anhydrous 5-aminotetrazole, and the new mixture is stirred at reflux for an additional 16 hours. Cooling to room temperature results in precipitation of 3-methoxy-5-phenyl-N- 1H-tetrazol-5-yl-2-benzofurancarboxamide. The precipitate is filtered and recrystallized from methanol to yield 0.90 g 80% yield) of analytically pure tetrazole, mp 260°-262° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04703053 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-62f2d69d5b034f1792dd830d4a3cbd46 |
| Source note | uspto-grants-1987_10 |