Phenol → (2,2-Diethoxyethoxy)benzene

HRID 6435

反応式

HRID 6435 の反応式
[H-].[Na+].[C:3]1([OH:9])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:10]([O:12][CH:13]([O:16][CH2:17][CH3:18])[CH2:14]Br)[CH3:11]>CN1C(=O)N(C)CCC1>[CH2:10]([O:12][CH:13]([O:16][CH2:17][CH3:18])[CH2:14][O:9][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1)[CH3:11]

参加物

5

反応条件

温度
110 °C

実験手順

Sodium hydride (5.83 g of a 55% dispersion in mineral oil) was added to a solution of phenol (12.56 g) in DMPU (25 ml) at 5° C. and the mixture was stirred for 30 minutes. Bromoacetaldehyde diethyl acetal (10.05 ml) was added and the mixture was heated at 110° C. for 5 hours, then allowed to cool. The mixture was partitioned between ethyl acetate (100 ml) and water (100 ml) and the organic phase was separated and washed sequentially with aqueous 2M sodium hydroxide solution (2×50 ml) and water (50 ml). The aqueous fractions were combined and re-extracted with ethyl acetate (100 ml). The combined organic extracts were dried (MgSO4) and concentrated. The resultant oil was purified by flash column chromatography, eluting with ethyl acetate/hexane (1:10 v/v) to give 2-phenoxyacetaldehyde diethyl acetal (9.43 g) as an oil; NMR: 1.25(6H,t, J=7.0 Hz), 3.6-3.85(4H,m), 4.05(2 H,d, J=6.0 Hz), 4.85 (1H,t, J=6.0 Hz) and 6.9-7.35(5H,m).

後処理

  1. temperatureto cool
  2. customThe mixture was partitioned between ethyl acetate (100 ml) and water (100 ml)
  3. customthe organic phase was separated
  4. washwashed sequentially with aqueous 2M sodium hydroxide solution (2×50 ml) and water (50 ml)
  5. extractionre-extracted with ethyl acetate (100 ml)
  6. dry with materialThe combined organic extracts were dried (MgSO4)
  7. concentrationconcentrated
  8. customThe resultant oil was purified by flash column chromatography
  9. washeluting with ethyl acetate/hexane (1:10 v/v)

出典と根拠

ORDレコード
ord-db8a01301d8543ea840e78a021d649d8
出典データセット
uspto-grants-1993_09
特許番号
US05248780

関連ノート

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