2,5-Dichlorobenzoyl chloride → Benzoyl chloride, 3,4-dichloro-
반응식
[Cl:1]C1C=C([N+]([O-])=O)C=CC=1C(Cl)=O.BrC1C=C(C=CC=1C)C(Cl)=O.FC1C=CC=C(F)C=1C(Cl)=O.Cl[C:37]1[CH:45]=[CH:44][C:43]([Cl:46])=[CH:42][C:38]=1[C:39]([Cl:41])=[O:40].ClC1C=C(C=C(Cl)C=1)C(Cl)=O.C1(C(Cl)=O)C2C(=CC=CC=2)C=CC=1>>[Cl:46][C:43]1[CH:42]=[C:38]([CH:37]=[CH:45][C:44]=1[Cl:1])[C:39]([Cl:41])=[O:40]참가 물질
7
실험 절차
Similarly, substituting 2-chloro-4-nitrobenzoyl chloride, 3-bromo-4-methylbenzoyl chloride, 2,6-difluorobenzoyl chloride, 2,5-dichlorobenzoyl chloride, 3,5-dichlorobenzoyl chloride or naphthoyl chloride, for 3,4-dichlorobenzoyl chloride, yields respectively: 2-chloro-4-nitrobenzoic acid, 2-(tert)-butylhydrazide; 3-bromo-4-methylbenzoic acid, 2-(tert)-butylhydrazide; mp 95°-97° C.; 2,5-dichlorobenzoic acid 2-(tert)-butylhydrazide and 3,5dichlorobenzoic acid, 2-(tert)-butylhydrazide, mp 163°-165° C.; 1-naphthoic acid, 2-(tert)-butylhydrazide mp 148°-150° C.
출처 및 근거
- ORD 기록
- ord-2d1632d7aaae41f482e08320e8bf065d
- 출처 데이터셋
- uspto-grants-1989_03
- 특허 번호
- US04814349
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