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Iodine → 6-Acetyl-2-chloro-3-hydroxy-4-iodo-pyridine

HRID 1637784
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HRID 1637784 반응식
[Cl:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[C:4]([CH:9]([OH:11])[CH3:10])[N:3]=1.C(=O)([O-])[O-].[K+].[K+].[I:18]I>O>[C:9]([C:4]1[N:3]=[C:2]([Cl:1])[C:7]([OH:8])=[C:6]([I:18])[CH:5]=1)(=[O:11])[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 807IodineHCID 11430Potassium CarbonateHCID 106073192-Chloro-6-(1-hydroxyethyl)pyridin-3-ol

생성물 1

HCID 187995586-Acetyl-2-chloro-3-hydroxy-4-iodo-pyridine수율 38%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

2-Chloro-3-hydroxy-6-(1-hydroxyethyl)pyridine (7.19 g, 41.4 mmole) was dissolved in 80 ml of water containing potassium carbonate (17.2 g, 124 mmole) in a 200 ml one neck round bottom flask. The solution was treated with iodine (31.5 g, 124 mmole) and was stirred for 6 h at room temperature. The mixture was quenched with saturated sodium thiosulfate and the pH was adjusted to 2 with 12 N hydrochloric acid. The precipitate was collected, was washed with water, and was dried. The yellow solid was further washed with diethyl ether to provide 4.68 g (38%) of 6-acetyl-2-chloro-3-hydroxy-4-iodo-pyridine as a pale tan solid (Melting Point: 223-224° C.).

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후처리

  1. customThe mixture was quenched with saturated sodium thiosulfate
  2. customThe precipitate was collected
  3. washwas washed with water
  4. customwas dried
  5. washThe yellow solid was further washed with diethyl ether

출처 및 근거

ORD 기록
ord-cca06b3cbe44485ab41416bb2b764df4
출처 데이터셋
uspto-grants-2000_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06043248

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