HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 23677909, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | ethyl 1-(4-methoxybenzyl)-1H-tetrazole-5-carboxylate | HCID 11097352 | — |
| Reactant | ethyl 2-(4-methoxybenzyl)-2H-tetrazole-5-carboxylate | HCID 13596243 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23677909 | HCID 23677909 | 35.4% |
Reaction Steps
A mixture of ethyl 1-(4-methoxybenzyl)-1H-tetrazole-5-carboxylate and ethyl 2-(4-methoxybenzyl)-2H-tetrazole-5-carboxylate (11.7 g) (prepared as described below and still containing a little sulpholane) was dissolved in hot ethanol (165 ml) and the solution was treated with a solution of potassium hydroxide (4.5 g) in water (13.5 ml). The mixture was cooled and the white crystalline solid which separated was filtered off to give potassium 2-(4-methoxybenzyl)-2H-tetrazole-5-carboxylate (4.3 g), m.p. 271°-273° C. (with decomposition). [The pure salt, obtained as a hemihydrate after recrystallisation from water, had a melting point of 273°-274° C. (with decomposition)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04442115 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-a3da7f7cff57400b8998478f56beea94 |
| Source note | uspto-grants-1984_04 |