HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bendazac → [(1-Benzyl-1H-indazol-3-yl)oxy]acetyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bendazac | HCID 2313 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | [(1-Benzyl-1H-indazol-3-yl)oxy]acetyl chloride | HCID 21486343 | 90% |
Reaction Steps
[(1-BENZYL-1H-indazol-3-yl)-oxy]acetic acid (Bendazac) (50 g) are suspended in benzene (500 ml) and thionyl chloride (15 ml) is added. The solution is stirred under reflux for about half an hour, cooled, concentrated at room temperature under reduced pressure, the oily residue is treated with further benzene and concentrated again to dryness under vacuum. After addition of hexane, the acidic chloride precipitates as lightly coloured crystals. The solution is filtered and washed with hexane. The substance is colourless and shows m.p. 78°-9°. Yield: 90% of the calculated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04001219 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-924798faf7fc4835bb271cf9a2d79154 |
| Source note | uspto-grants-1977_01 |