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4-Formylbenzoic acid → HCID 59811331、化合物

HRID 2102881
ノート
印刷プレビュー

反応式

HRID 2102881 の反応式
[C:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1)([OH:3])=[O:2].[CH2:12]([Mg]Cl)[C:13]([CH3:16])([CH3:15])[CH3:14]>C1COCC1.CCCCCC>[CH3:12][C:13]([CH3:16])([CH3:15])/[CH:14]=[CH:8]/[C:7]1[CH:10]=[CH:11][C:4]([C:1]([OH:3])=[O:2])=[CH:5][CH:6]=1
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 120884-Formylbenzoic acidHCID 178418809HCID 178418809、化合物

生成物 1

HCID 59811331HCID 59811331、化合物

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 8058Hexane溶媒

実験手順

To a cooled (0° C.) and well stirred suspension of 4-carboxy benzaldehyde (2.0 g, 13.32 mmol) in anhydrous THF (90 mL) is added 33.3 mmol of neopentyl magnesium chloride in hexane during 20 minutes and the mixture is stirred at the same temperature for an additional two hours before being quenched with satyrated ammonium chloride solution. Most of the THF is evaporated and the aqueous mixture is treated with conc. HCl (50 mL) and the mixture is heated to reflux for 2 hours. The mixture is then cooled to ambient temperature and extracted with methylene chloride (2×100 mL), the organic layer is dried over sodium sulfate and concentrated to obtain the desired compound.

後処理

  1. temperatureTo a cooled
  2. custombefore being quenched with satyrated ammonium chloride solution
  3. customMost of the THF is evaporated
  4. additionthe aqueous mixture is treated with conc. HCl (50 mL)
  5. temperaturethe mixture is heated
  6. temperatureto reflux for 2 hours
  7. extractionextracted with methylene chloride (2×100 mL)
  8. dry with materialthe organic layer is dried over sodium sulfate
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-bac294cdee2044a5807845b90ebb8f8e
出典データセット
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07576099B2

反応ノート

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