反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][C:12]=2[Cl:21])=[CH:6][C:5]=1[CH2:22][CH2:23][O:24][NH2:25])([O-:3])=[O:2].ClC1C=C(C(F)(F)F)C=CC=1OC1C=CC([N+]([O-])=O)=C([N+]([O-])=O)C=1.Cl.C(ON)C.C1(CCON)C=CC=CC=1.Br[CH2:66][C:67]([O:69][CH3:70])=[O:68]>>[CH3:70][O:69][C:67]([CH2:66][NH:25][O:24][CH2:23][CH2:22][C:5]1[CH:6]=[C:7]([O:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:18])([F:19])[F:20])=[CH:13][C:12]=2[Cl:21])[CH:8]=[CH:9][C:4]=1[N+:1]([O-:3])=[O:2])=[O:68]参加物
6
実験手順
Following the procedure of Example 29, N-[2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenyl]ethoxyamine is prepared from 4-(2-chloro-4-trifluoromethylphenoxy)1,2-dinitrobenzene and ethoxyamine hydrochloride. The resulting N-phenylethoxyamine is then reacted with methyl bromoacetate, following the methods of this example, to yield N-methoxycarbonylmethyl-N-[2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenyl]ethoxyamine.
出典と根拠
- ORDレコード
- ord-c15788ec88a2485daccd358bdb82bb9a
- 出典データセット
- uspto-grants-1985_07
- 特許番号
- US04526608
関連ノート
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