Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde oxime → 4-Chloro-benzaldehyde oxime
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-(1,1,2,2-Tetrafluoroethoxy)benzaldehyde oxime | HCID 85531600 | — |
| 반응물 | HCID 178479532 | HCID 178479532 | — |
| 생성물 | 4-Chloro-benzaldehyde oxime | HCID 219158 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04649148 |
| 출처 데이터셋 | uspto-grants-1987_03 |
| ORD ID | ord-7595c8efa3f048ef868d25ee45b7ffca |
| 출처 메모 | uspto-grants-1987_03 |