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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414162Generated: November 1, 2026

Bendazac → [(1-Benzyl-1H-indazol-3-yl)oxy]acetyl chloride

https://huagongshe.com/reaction/1414162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBendazacHCID 2313—
ReactantThionyl ChlorideHCID 24386—
SolventBenzeneHCID 241—
Product[(1-Benzyl-1H-indazol-3-yl)oxy]acetyl chlorideHCID 2148634390%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001219
Source datasetuspto-grants-1977_01
ORD IDord-924798faf7fc4835bb271cf9a2d79154
Source noteuspto-grants-1977_01