反応式
[Cl:1][C:2]1[CH:20]=[C:19]([C:21]([F:24])([F:23])[F:22])[CH:18]=[CH:17][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[C:7]([N+]([O-])=O)[CH:6]=1.ClC1C([N+]([O-])=O)C(C2C=CC=CC=2C(F)(F)F)([N+]([O-])=O)C=CC=1OC1C=CC([N+]([O-])=O)(C2C=CC=CC=2C(F)(F)F)C([N+]([O-])=O)C=1Cl.[CH3:72][P:73]([O:76]C)[O:74][CH3:75]>C(#N)C>[CH3:72][P:73]([C:7]1[CH:6]=[C:5]([O:4][C:3]2[CH:17]=[CH:18][C:19]([C:21]([F:24])([F:23])[F:22])=[CH:20][C:2]=2[Cl:1])[CH:10]=[CH:9][C:8]=1[N+:11]([O-:13])=[O:12])(=[O:76])[O:74][CH3:75]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of 4-(2-chloro-4-trifluoromethylphenoxy)-1,2-dinitrobenzene, (2-chloro-α,α,α-trifluoro-p-tolyl-3,4-dinitrophenyl ether) (1.2 g, 3.31 mmol) and dimethyl methylphosphonite (0.57 g, 5.3 mmol) in 3 ml of acetonitrile is refluxed overnight. The mixture is concentrated and the residue is purified by column chromatography (silica gel, eluting with 3% ethyl acetate/hexane) to yield methyl P-methyl-2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenylphosphinate.
後処理
- temperatureis refluxed overnight
- concentrationThe mixture is concentrated
- customthe residue is purified by column chromatography (silica gel, eluting with 3% ethyl acetate/hexane)
出典と根拠
- ORDレコード
- ord-3db1e4a4f26946b285cbce4977c51fba
- 出典データセット
- uspto-grants-1986_01
- 特許番号
- US04563310
関連ノート
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