Hydrochloric Acid → 4-Fluoro-2,3-dihydroxybenzaldehyde

HRID 218257

反応式

HRID 218257 の反応式
[Cl-].[Mg+2].[Cl-].[F:4][C:5]1[CH:11]=[CH:10][CH:9]=[C:7]([OH:8])[C:6]=1[OH:12].C(N(CC)CC)C.[CH2:20]=[O:21].Cl>C(#N)C.CC(OC)(C)C>[F:4][C:5]1[CH:11]=[CH:10][C:9]([CH:20]=[O:21])=[C:7]([OH:8])[C:6]=1[OH:12]

参加物

8

実験手順

Magnesium chloride (3.71 g, 33 mmol) was added portionwise at room temperature to a solution of 3-fluorocatechol (2 g, 15.6 mmol) in acetonitrile (20 mL), followed by triethylamine (13.4 mL, 97.5 mmol). Paraformaldehyde (3.16 g, 105.3 mmol) was then added to the stirred suspension and the mixture was heated at reflux for 5 hours. The mixture was cooled to room temperature then poured into a mixture of 5% HCl and TBME. The organic phase was separated, and the aqueous layer re-extracted with TBME. The combined organic extracts were washed with brine, dried over sodium sulphate and the solvent removed under reduced pressure. The crude mixture (˜1:1 starting material:product) was purified on normal silica in neat DCM followed by DCM/MeOH 96:4 and 90:10 to yield 478 mg of 28 still contaminated with 11.4% w/w of 3-fluorocatechol.

後処理

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 5 hours
  3. customThe organic phase was separated
  4. extractionthe aqueous layer re-extracted with TBME
  5. washThe combined organic extracts were washed with brine
  6. dry with materialdried over sodium sulphate
  7. customthe solvent removed under reduced pressure
  8. customThe crude mixture (˜1:1 starting material:product) was purified on normal silica in neat DCM

出典と根拠

ORDレコード
ord-87e79cbc614f479d95cef12d52eb50aa
出典データセット
uspto-grants-2012_06
特許番号
US08198302B2

関連ノート

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