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

HRID 854985
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HRID 854985 반응식
[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]
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참가 물질

5

반응물 3

HCID 962WaterHCID 24526Chlorine2회HCID 2526125-Iodosalicylaldehyde

생성물 1

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

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
70 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-db4fbbff74724251ae682e5bb1080793
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07259266B2

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