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Water → 3-Chloro-2-hydroxy-5-iodobenzaldehyde

HRID 854985
ノート
印刷プレビュー

反応式

HRID 854985 の反応式
[I:1][C:2]1[CH:9]=[C:6]([CH:7]=[O:8])[C:5]([OH:10])=[CH:4][CH:3]=1.[Cl:11]Cl.O>C(O)(=O)C>[Cl:11][C:4]1[C:5]([OH:10])=[C:6]([CH:9]=[C:2]([I:1])[CH:3]=1)[CH:7]=[O:8]
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

5

反応物 3

HCID 962WaterHCID 24526Chlorine2 回HCID 2526125-Iodosalicylaldehyde

生成物 1

HCID 589350053-Chloro-2-hydroxy-5-iodobenzaldehyde

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
70 °C

実験手順

To 24 g (96.8 mmole) of 5-iodosalicylaldehyde in 320 mL of acetic acid was added an excess of gaseous chlorine. After addition of about 10 g of Cl2, a white solid appeared in the solution. The mixture was heated to 70° C. and allowed to stir for 3 h. The heated solution was homogeneous and remained so after cooling to rt. The mixture was added to 1200 mL of water and allowed to stir for 1 h. The resultant solid was collected by filtration, washed with water, filtered and allowed to air dry to afford 27.3 g of a yellow solid. The solid was recrystallized by dissolving the material in 250 mL of hot methanol and adding 80 mL of H2O. After standing overnight, the crystalline solid was collected and air-dried to afford 20.3 g (74.2%) of a yellow solid. The product contained a minor impurity (approx. 9% by 1H NMR) and was used in the next step without further purification: 1H NMR (CDCl3/400 MHz) 7.78 (d, 1H, J=2.1 Hz), 7.88 (d, 1H, J=1.8 Hz), 9.83 (s, 1H), 11.40 (s, 1H); 13C NMR (CDCl3/100 MHz) 79.5, 122.8, 123.7, 140.3, 144.4, 156.9, 194.8; MS (ESI+) 283 (M+1, 100); HRMS (El) m/z calcd for (C7H4O2ICl) 281.8945, found 281.8899.

後処理

  1. temperatureafter cooling to rt
  2. stirringto stir for 1 h
  3. filtrationThe resultant solid was collected by filtration
  4. washwashed with water
  5. filtrationfiltered
  6. customto air dry

出典と根拠

ORDレコード
ord-db4fbbff74724251ae682e5bb1080793
出典データセット
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07259266B2

反応ノート

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