Phenol → (2,2-Diethoxyethoxy)benzene

HRID 373955

Reaction equation

HRID 373955 reaction equation
[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]

Participants

5

Conditions

Temperature
110 °C

Procedure

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).

Workup

  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)

Sources & evidence

ORD record
ord-a198baa2980a4339a8a3dd158c99fde3
Source dataset
uspto-grants-1992_11
Patent number
US05166213

Linked notes

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