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Nitric Acid → 3-Nitro-4-(propan-2-yl)aniline

HRID 924667
ノート
印刷プレビュー

反応式

HRID 924667 の反応式
[CH3:1][CH:2]([C:4]1[CH:10]=[CH:9][C:7]([NH2:8])=[CH:6][CH:5]=1)[CH3:3].S(=O)(=O)(O)O.[N+:16]([O-])([OH:18])=[O:17]>>[N+:16]([C:5]1[CH:6]=[C:7]([CH:9]=[CH:10][C:4]=1[CH:2]([CH3:3])[CH3:1])[NH2:8])([O-:18])=[O:17]
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 3

HCID 944Nitric AcidHCID 1118Sulfuric Acid2 回HCID 74644-Isopropylaniline

生成物 1

HCID 221118273-Nitro-4-(propan-2-yl)aniline収率 71%

反応条件

温度
8 °C

実験手順

4-(Propan-2-yl)aniline (10.12 mL, 74 mmol) was added drop wise to sulfuric acid (96%, 57 mL), cooled to 8° C., maintaining the temperature below 10° C. After the addition, the reaction mixture was cooled to −5° C., before the addition of a mixture of nitric acid (100%, 3.7 mL) and sulfuric acid (96%, 9 mL), keeping the temperature below 0° C. The reaction mixture was then stirred at the same temperature for 1 h. The reaction mixture was poured into ice (200 mL) and the precipitate filtered and washed with water. The solid was suspended with water (100 mL) and neutralized with ammonium hydroxide (35%). The precipitate was filtered and dried in the oven to obtain a light-brown solid (9.49 g, 71%).

後処理

  1. temperaturemaintaining the temperature below 10° C
  2. additionAfter the addition
  3. customthe temperature below 0° C
  4. filtrationthe precipitate filtered
  5. washwashed with water
  6. filtrationThe precipitate was filtered
  7. customdried in the oven

出典と根拠

ORDレコード
ord-ad3a2789617842f9827bdf3f20777e83
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09283224B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート