Triethanolamine → Tris-(2-hydroxyethyl)ammonium 5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate

HRID 27321

反応式

HRID 27321 の反応式
[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:6]=[CH:7][C:8]([N+:14]([O-:16])=[O:15])=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11].[N:25]([CH2:32][CH2:33][OH:34])([CH2:29][CH2:30][OH:31])[CH2:26][CH2:27][OH:28]>C(COC)OC>[Cl:1][C:2]1[CH:20]=[C:19]([C:21]([F:22])([F:23])[F:24])[CH:18]=[CH:17][C:3]=1[O:4][C:5]1[CH:6]=[CH:7][C:8]([N+:14]([O-:16])=[O:15])=[C:9]([CH:13]=1)[C:10]([O-:12])=[O:11].[OH:28][CH2:27][CH2:26][NH+:25]([CH2:32][CH2:33][OH:34])[CH2:29][CH2:30][OH:31]

参加物

4

実験手順

5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzoic acid (3.0 g, 0.0083 mole) is dissolved in glyme (20 ml) and a solution of triethanolamine (1.35 g, 0.0091 mole) in glyme (5 ml) is added rapidly while stirring at room temperature. After stirring for a few hours the solvent is removed in vacuo, the product is triturated repeatedly with petroleum ether (bp 30°-60° C.) and dried to a weight of 2.5 g.

後処理

  1. stirringAfter stirring for a few hours the solvent
  2. customis removed in vacuo
  3. customthe product is triturated repeatedly with petroleum ether (bp 30°-60° C.)
  4. customdried to a weight of 2.5 g

出典と根拠

ORDレコード
ord-15498aed66e54dc2a770e565828a381f
出典データセット
uspto-grants-1980_09
特許番号
US04220468

関連ノート

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