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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22156Generated: October 29, 2026

6-[(2-Chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-alpha-methyl-1h-benzotriazole-1-acetaldehyde oxime → 6-[(2-chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-alpha-methyl-1H-benzotriazole-1-acetonitrile

https://huagongshe.com/reaction/22156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-[(2-Chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-alpha-methyl-1h-benzotriazole-1-acetaldehyde oximeHCID 86747946—
SolventAcetic AnhydrideHCID 7918—
Product6-[(2-chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-alpha-methyl-1H-benzotriazole-1-acetonitrileHCID 86748751—

Reaction Steps

A solution of 6-[(2-chloro-α,α,α,6-tetrafluoro-p-tolyl)oxy]-α-methyl-1H-benzotriazole-1-acetaldehyde oxime (5.0 g, 0.012 mol) in acetic anhydride is allowed to stand at 22° C. for 20 hours and concentrated in vacuo to give an oil residue. The residue is chromatographed on silica gel using chloroform as eluant to afford the title compound (I), 2.0 g, mp 118°-119° C., identified by elemental and NMR analyses and the title compound (II), 2.1 g, mp 95°-97° C., identified by elemental and NMR analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428003
Source datasetuspto-grants-1995_06
ORD IDord-740ebc5713fb441d9ef7f34b8b84787a
Source noteuspto-grants-1995_06