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Sodium Bicarbonate → Methyl 2-(2,6-difluoro-4-methoxyphenyl)acetate

HRID 82787
ノート
印刷プレビュー

反応式

HRID 82787 の反応式
[F:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[C:4]([F:10])[C:3]=1[CH2:11][C:12]([OH:14])=[O:13].[C:15]([O-])(O)=O.[Na+]>CO.Cl>[F:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[C:4]([F:10])[C:3]=1[CH2:11][C:12]([O:14][CH3:15])=[O:13]
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 2

HCID 516892Sodium BicarbonateHCID 51873792-(2,6-Difluoro-4-methoxyphenyl)acetic acid

生成物 1

HCID 67043009Methyl 2-(2,6-difluoro-4-methoxyphenyl)acetate収率 92%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid触媒HCID 887Methanol溶媒

実験手順

A solution of PMW04140 (3.37 g, 16.7 mmol) in MeOH (70 mL) containing conc. HCl (15 drops) was heated at reflux overnight. The mixture was allowed to cool and was neutralised with sat aq. NaHCO3. The solvent was removed in vacuo and the residue was dissolved in EtOAc (100 mL) and washed with H2O (100 mL), sat. aq, NaHCO3 (100 mL) and brine (100 mL) then dried (MgSO4) and the solvent was removed in vacuo. The title compound (3.30 g, 92%) was obtained as a pale yellow oil; 1H NMR. (270 MHz, DMSO-d6) 3.61 (2H, s, CH2), 3.69 (3H, s, CH3), 3.76 (3H, s, CH3), 6.40-6.49 (2H, m, ArH); 19F NMR (376.4 MHz, DMSO-d6)-114.4 (d); HRMS (ES+) calcd, for C10H11F2O3 (M++H) 217.0657. found 217.0663; LC/MS (ES+) tr=1.69 min, m/z 216.8 (M+, 100%).

後処理

  1. temperaturewas heated
  2. temperatureat reflux overnight
  3. temperatureto cool
  4. customThe solvent was removed in vacuo
  5. dissolutionthe residue was dissolved in EtOAc (100 mL)
  6. washwashed with H2O (100 mL)
  7. dry with materialsat. aq, NaHCO3 (100 mL) and brine (100 mL) then dried (MgSO4)
  8. customthe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-3142bc87fd51444c9d09642cbbdeaea9
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08846737B2

反応ノート

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