HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicyloyl chloride → HCID 178513857, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicyloyl chloride | HCID 74041 | — |
| Reactant | HCID 178514233 | HCID 178514233 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178513857 | HCID 178513857 | — |
Reaction Steps
A 25 ml. portion of dry acetonitrile is added to a mixture of 1.3 g. of the s-triazole carboxamide sodium salt and 2 g. of salicyloyl chloride followed by a few pellets of 4A molecular sieves. The mixture is stirred at room temperature for 16 hours and then filtered through Celite. The colorless solid is obtained on evaporating the filtrate is washed with diethyl ether; yield, 1 g., m.p. 147°-150° C. (dec.). Its infrared spectrum is essentially the same as that obtained from the product in Example 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006159 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-fc5a8c5d9c524162bb776eeae08319f4 |
| Source note | uspto-grants-1977_02 |