Ammonia → 4-Methyl-5-nitrosaccharin

HRID 1599972ノート

反応式

HRID 1599972 の反応式
[NH3:1].O.C[O:4][C:5]([C:7]1[C:12]([CH3:13])=[C:11]([N+:14]([O-:16])=[O:15])[CH:10]=[CH:9][C:8]=1[S:17](Cl)(=[O:19])=[O:18])=O>O1CCCC1>[CH3:13][C:12]1[C:11]([N+:14]([O-:16])=[O:15])=[CH:10][CH:9]=[C:8]2[C:7]=1[C:5](=[O:4])[NH:1][S:17]2(=[O:19])=[O:18]

参加物

5

反応条件

温度
25 °C

実験手順

104 ml of 25 percent ammonia solution are initially taken, 100 ml of water are added and a solution of 48.7 g (0.166 mol) of 2-methoxycarbonyl-3-methyl-4-nitrobenzenesulfonyl chloride in 70 ml of tetrahydrofuran is then added dropwise at 10° C. After stirring at 25° C. for three hours, water and THF are largely removed and the residue which remains is stirred with ethyl acetate, filtered off with suction and washed with ethyl acetate. After drying under reduced pressure, 34 g (0.131 mol)=79% of theory of a white solid of m.p.: 312° C. (dec.) are obtained.

後処理

  1. customwater and THF are largely removed
  2. stirringthe residue which remains is stirred with ethyl acetate
  3. filtrationfiltered off with suction
  4. washwashed with ethyl acetate
  5. customAfter drying under reduced pressure, 34 g (0.131 mol)=79% of theory of a white solid of m.p.: 312° C. (dec.)
  6. customare obtained

出典と根拠

ORDレコード
ord-ec3e47225e444bbdb1271612591fff07
出典データセット
uspto-grants-1998_04
特許番号
US05744425

反応ノート

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