2,3-Diisopropoxy-4-methoxybenzaldehyde → 2,3-Diisopropoxy-1-(1-hydroxyethyl)-4-methoxybenzene

HRID 9309

反応式

HRID 9309 の反応式
[CH:1]([O:4][C:5]1[C:12]([O:13][CH:14]([CH3:16])[CH3:15])=[C:11]([O:17][CH3:18])[CH:10]=[CH:9][C:6]=1[CH:7]=[O:8])([CH3:3])[CH3:2].[CH3:19][Li]>C(OCC)C>[CH:1]([O:4][C:5]1[C:12]([O:13][CH:14]([CH3:16])[CH3:15])=[C:11]([O:17][CH3:18])[CH:10]=[CH:9][C:6]=1[CH:7]([OH:8])[CH3:19])([CH3:3])[CH3:2]

参加物

4

反応物 2

HCID 219865542,3-Diisopropoxy-4-methoxybenzaldehydeHCID 178418348HCID 178418348、化合物

生成物 1

HCID 219865522,3-Diisopropoxy-1-(1-hydroxyethyl)-4-methoxybenzene収率 84%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

To a solution of 22 (23.10 g, 91.56 mmol) in dry ethyl ether (150 mL) was added dropwise methyllithium (98.10 mL, 1.4 M in EtO2, 1.37.3 mmol) at 0° C. under nitrogen. The reaction mixture was stirred for 2 h allowing too reach room temperature. The reaction was slowly quenched with water, the phases were separated, and the aqueous phase was extracted with ethyl ether (3×150 mL). The combined organic solutions were dried over MgSO4 and concentrated over reduced pressure. Purification by flash column chromatography (silica gel, elution with hexanes/EtOAc: 80/20) provided the protected alcohol 20.62 g (76.77 mmol, 84%) as a pale yellow oil.

後処理

  1. customallowing too reach room temperature
  2. customThe reaction was slowly quenched with water
  3. customthe phases were separated
  4. extractionthe aqueous phase was extracted with ethyl ether (3×150 mL)
  5. dry with materialThe combined organic solutions were dried over MgSO4
  6. concentrationconcentrated over reduced pressure
  7. customPurification
  8. washby flash column chromatography (silica gel, elution with hexanes/EtOAc: 80/20)

出典と根拠

ORDレコード
ord-984178fe26d140788905778d11aa6935
出典データセット
uspto-grants-2006_08
特許番号
US07091240B2

関連ノート

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