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

HRID 1637784
ノート
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反応式

HRID 1637784 の反応式
[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]
参加物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 807IodineHCID 11430Potassium CarbonateHCID 106073192-Chloro-6-(1-hydroxyethyl)pyridin-3-ol

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-cca06b3cbe44485ab41416bb2b764df4
出典データセット
uspto-grants-2000_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06043248

反応ノート

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