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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905930Generated: October 25, 2026

p-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde oxime → 4-Chloro-benzaldehyde oxime

https://huagongshe.com/reaction/1905930

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde oximeHCID 85531600—
ReactantHCID 178479532HCID 178479532—
Product4-Chloro-benzaldehyde oximeHCID 219158—

Reaction Steps

Using a similar procedure, 1-amino-3-p{[p-(1,1,2,2-tetrafluoroethoxy)benzylidene]amino}guanidine hydrochloride (white solid, mp 205°-212° C.); 1-amino-3-{p-(trifluoroethoxy)benzylidene]amino}guanidine hydrochloride (white powder; mp 235°-238° C.); and 1-amino-3-(p-chlorobenzylideneamino)guanidine hydrochloride may be prepared. The second products of the reactions, p-(1,1,2,2-tetrafluoroethoxy)benzaldehyde oxime (pinkish white solid, mp 47°-53.5° C.); α,α,α-trifluoro-p-anilaldehyde oxime (off-white solid, mp 46°-49.5° C.) and p-chlorbenzaldehyde oxime may also be isolated from the reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04649148
Source datasetuspto-grants-1987_03
ORD IDord-7595c8efa3f048ef868d25ee45b7ffca
Source noteuspto-grants-1987_03