HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde oxime → 4-Chloro-benzaldehyde oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde oxime | HCID 85531600 | — |
| Reactant | HCID 178479532 | HCID 178479532 | — |
| Product | 4-Chloro-benzaldehyde oxime | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04754067 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-ad2bda4939a1432b818e76218c461f98 |
| Source note | uspto-grants-1988_06 |