Tetrahydrofuran → N-methyl-N-[2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenyl]acetoxymethoxyamine
반응식
CN(O)[C:3]1[CH:8]=[C:7]([O:9][C:10]2[CH:15]=[CH:14][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:12][C:11]=2[Cl:20])[CH:6]=[CH:5][C:4]=1[N+:21]([O-:23])=[O:22].C([N:27]([CH2:30]C)CC)C.Cl[CH2:33][O:34][C:35](=[O:37])[CH3:36].C1C[O:41]CC1>>[CH3:30][NH:27][O:41][CH2:33][O:34][C:35](=[O:37])[CH2:36][C:3]1[CH:8]=[C:7]([O:9][C:10]2[CH:15]=[CH:14][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:12][C:11]=2[Cl:20])[CH:6]=[CH:5][C:4]=1[N+:21]([O-:23])=[O:22]참가 물질
5
실험 절차
To a solution of N-methyl-N-[2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenyl]hydroxyamine (700 mg, 1.93 mmol) in THF (10 ml) containing triethylamine (1.2 eq.) is added chloromethylacetate (2 eq.). The mixture is stirred at RT overnight. Excess THF is removed and the product is evaporated to dryness and purified to give N-methyl-N-[2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenyl]acetoxymethoxyamine.
후처리
- customExcess THF is removed
- customthe product is evaporated to dryness
- custompurified
출처 및 근거
- ORD 기록
- ord-06264be53c1c4997ae34a1e86f5bd9a6
- 출처 데이터셋
- uspto-grants-1985_07
- 특허 번호
- US04526608
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