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Urea → Benzene, 1,3-dichloro-2-iodo-5-nitro-

HRID 35287
ノート
印刷プレビュー

反応式

HRID 35287 の反応式
[Cl:1][C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[CH:6]=[C:5]([Cl:12])[C:3]=1N.N([O-])=O.[Na+].NC(N)=O.[I-:21].[K+]>C(O)(=O)C.S(=O)(=O)(O)O.O>[Cl:1][C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[CH:6]=[C:5]([Cl:12])[C:3]=1[I:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 1176UreaHCID 4875Potassium IodideHCID 74302,6-Dichloro-4-nitroanilineHCID 23668193Sodium Nitrite

生成物 1

HCID 112948Benzene, 1,3-dichloro-2-iodo-5-nitro-収率 86%

試薬・触媒・溶媒 3

HCID 176Acetic Acid溶媒
HCID 962
Water
溶媒
HCID 1118Sulfuric Acid溶媒

実験手順

To a stirred suspension of 2,6-dichloro-4-nitroaniline (200 g) in glacial acetic acid (1.3 l) at 16° was added dropwise a solution of sodium nitrite (93.84 g) in concentrated sulphuric acid (500 ml), keeping the reaction mixture below 22°. The reaction mixture was stirred and kept below this temperature for 0.5 hour, then poured slowly onto crushed ice/water (2.5 liters) containing urea (31.71 g), keeping the mixture below 23°. Potassium iodide (225.77 g) in water (600 ml) was slowly added with stirring and the mixture stirred at room temperature for 3 hours. The product was filtered off, washed with water then triturated with hot ethanol to give 3,5-dichloro-4-iodonitrobenzene (263.4 g, 86%) as a buff solid, m.p. 147°-150°.

後処理

  1. customthe reaction mixture below 22°
  2. additionpoured slowly
  3. customthe mixture below 23°
  4. stirringwith stirring
  5. stirringthe mixture stirred at room temperature for 3 hours
  6. filtrationThe product was filtered off
  7. washwashed with water
  8. customthen triturated with hot ethanol

出典と根拠

ORDレコード
ord-d40584a550694b0d8cc6ab48dd8e4ad1
出典データセット
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04766121

反応ノート

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