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Iodoethane → 2-Chloro-3-ethoxy-5-iodophenol

HRID 62763
ノート
印刷プレビュー

反応式

HRID 62763 の反応式
ICC.C([O-])([O-])=O.[K+].[K+].[C:10]([O:13][C:14]1[CH:19]=[C:18]([I:20])[CH:17]=[C:16]([OH:21])[C:15]=1[Cl:22])(=O)[CH3:11]>CN(C=O)C.C(OCC)C>[Cl:22][C:15]1[C:14]([O:13][CH2:10][CH3:11])=[CH:19][C:18]([I:20])=[CH:17][C:16]=1[OH:21]
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

6

反応物 3

HCID 6340IodoethaneHCID 11430Potassium Carbonate2 回HCID 670418062-Chloro-3-hydroxy-5-iodophenyl acetate

生成物 1

HCID 670422122-Chloro-3-ethoxy-5-iodophenol収率 58%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 6228Dimethylformamide
溶媒

反応条件

温度
60 °C

実験手順

Iodoethane (0.78 mL, 9.6 mmol) and K2CO3 (1.3 g, 9.6 mmol) were added to a solution of 2-chloro-3-hydroxy-5-iodophenyl acetate (6) (2.0 g, 6.4 mmol) in DMF (5 mL) and the mixture was stirred at 60° C. for 1 h. The reaction mixture was cooled to RT, diluted with diethyl ether (100 mL) and washed with brine (3×100 mL). The solvent was removed in vacuo and the residue was dissolved in MeOH (20 mL). K2CO3 (1.0 g, 7.2 mmol) was added and the mixture was stirred at RT for 20 h. The solvent was removed in vacuo and the residue was partitioned between EtOAc (100 mL) and water (100 mL). The organic layer was washed with water (100 mL) and evaporated in vacuo. The residue was purified by silica gel chromatography (40 g, 0-30% EtOAc in isohexane) to afford 2-chloro-3-ethoxy-5-iodophenol (7) (1.1 g, 58% yield) as a colourless solid: m/z 297 [M−H]− (ES−); 1H NMR (400 MHz, DMSO-d6) δ: 10.45 (1H, s), 6.89 (2H, d), 4.04 (2H, br s), 1.32 (3H, br s).

後処理

  1. temperatureThe reaction mixture was cooled to RT
  2. washwashed with brine (3×100 mL)
  3. customThe solvent was removed in vacuo
  4. dissolutionthe residue was dissolved in MeOH (20 mL)
  5. stirringthe mixture was stirred at RT for 20 h
  6. customThe solvent was removed in vacuo
  7. customthe residue was partitioned between EtOAc (100 mL) and water (100 mL)
  8. washThe organic layer was washed with water (100 mL)
  9. customevaporated in vacuo
  10. customThe residue was purified by silica gel chromatography (40 g, 0-30% EtOAc in isohexane)

出典と根拠

ORDレコード
ord-d513a6bb58c348e28669707b42ffd290
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09447028B2

反応ノート

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