HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 5-(Tetrazol-1-yl)-thiovaleric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 5-(Tetrazol-1-yl)-valeric acid chloride | HCID 17803406 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(Tetrazol-1-yl)-thiovaleric acid | HCID 178526188 | — |
Reaction Steps
5 g of 5-(tetrazol-1-yl)-valeric acid chloride are dissolved in 4.5 ml of absolute methylene chloride and, at 0°, this solution is added dropwise to 35.5 ml of a solution of pyridine and H2S in methylene chloride (30 ml of pyridine and 6 g of H2S in 100 ml of methylene chloride). The mixture is then stirred at 0° under a nitrogen atmosphere for 1 hour. The reaction mixture is taken up in chloroform, and the aqueous phase is acidified to pH 2 with 2N H2SO4 and extracted twice with chloroform. The combined organic phases are washed twice with 25 ml of 10% NaHCO3 solution. The pH is then adjusted to 3 with 2N H2SO4 and the title compound is obtained by repeated extraction with chloroform. It is dried over sodium sulphate and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04794109 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-ee5acc8b0d4344d4ba914b737018f4e7 |
| Source note | uspto-grants-1988_12 |