Nitric Acid → m-Nitrobenzenephosphonous acid
反応式
C1(P(Cl)Cl)C=CC=CC=1.[C:10]1([P:16]([OH:18])[OH:17])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[N+:19]([O-])([OH:21])=[O:20]>>[N+:19]([C:12]1[CH:11]=[C:10]([P:16]([OH:18])[OH:17])[CH:15]=[CH:14][CH:13]=1)([O-:21])=[O:20]参加物
実験手順
According to my invention phenylphosphorus dichloride is converted to benzenephosphonous acid (B), which is nitrated (I) with nitric acid at a temperature around 0° C. to form m-nitrobenzenephosphonous acid (E) which, to my knowledge, is a compound not previously described in the literature. Compound E is conveniently oxidized by heating (II) the reaction mixture in the presence of additional nitric acid to form m-nitrobenzenephosphonic acid (C), and then compound (D) by subsequent reduction. My contribution, then, includes the nitration of benzenephosphonous acid (B), which is considerably less costly than benzenephosphonic acid (A), to form the novel compound m-nitrobenzenephosphonous acid (E), followed by oxidation to form m-nitrobenzene phosphonic acid (C) which is converted by conventional reduction to form the desired m-aminobenzenephosphonic acid (D).
後処理
- customat a temperature around 0° C.
出典と根拠
- ORDレコード
- ord-9c65efd26ece43ae9c931f15cece7eeb
- 出典データセット
- uspto-grants-1977_06
- 特許番号
- US04028403
反応ノート
読み込み中…