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Nitric Acid → HCID 10379608、化合物

HRID 659986
ノート
印刷プレビュー

反応式

HRID 659986 の反応式
[C:1]([NH:4][C:5]1[C:6]([Cl:15])=[CH:7][C:8]([Cl:14])=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11])(=[O:3])[CH3:2].[N+:16]([O-])([OH:18])=[O:17]>S(=O)(=O)(O)O>[C:1]([NH:4][C:5]1[C:13]([N+:16]([O-:18])=[O:17])=[C:9]([C:8]([Cl:14])=[CH:7][C:6]=1[Cl:15])[C:10]([OH:12])=[O:11])(=[O:3])[CH3:2]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 944Nitric Acid2 回HCID 2833165-(Acetylamino)-2,4-dichlorobenzoic acid

生成物 1

HCID 10379608HCID 10379608、化合物収率 86%

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒2 回

反応条件

温度
0 °C

実験手順

5-Acetamido-2,4-dichlorobenzoic acid (1-4) (9.6 g, 0.039 mol) was added in small portions over 30 min to a stirred ice-cooled solution of fuming nitric acid (1.8 mL, 0.043 mol) and conc sulfuric acid (120 mL). After the addition was complete, more fuming nitric acid (17 mL) and conc sulfuric acid (80 mL) were added at 30 min and 60 min intervals. The reaction mixture was then left to stir for an additional 2.5 h at 0° C., allowed to warm to 12-16° C. and left to stir at this temperature until all starting material was consumed (about 3 h). The solution was poured onto ice and extracted with ethyl acetate (3×). The organic extracts were combined, washed with brine, dried, and concentrated to give 3-acetamido-4,6-dichloro-2-nitrobenzoic acid (1-5) as an orange solid (9.8 g, 86%).

後処理

  1. additionAfter the addition
  2. waitThe reaction mixture was then left
  3. temperatureto warm to 12-16° C.
  4. waitleft
  5. stirringto stir at this temperature until all starting material
  6. customwas consumed (about 3 h)
  7. additionThe solution was poured onto ice
  8. extractionextracted with ethyl acetate (3×)
  9. washwashed with brine
  10. customdried
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-6d33d0f9bebd412c80ecb2f7f4b8c951
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08084459B2

反応ノート

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