تفاعل #461137

ord-a198baa2980a4339a8a3dd158c99fde3

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
110°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto cool
  2. 2
    أخرىThe mixture was partitioned between ethyl acetate (100 ml) and water (100 ml)
  3. 3
    أخرىthe organic phase was separated
  4. 4
    غسيلwashed sequentially with aqueous 2M sodium hydroxide solution (2×50 ml) and water (50 ml)
  5. 5
    استخلاصre-extracted with ethyl acetate (100 ml)
  6. 6
    تجفيفThe combined organic extracts were dried (MgSO4)
  7. 7
    تركيزconcentrated
  8. 8
    أخرىThe resultant oil was purified by flash column chromatography
  9. 9
    غسيلeluting with ethyl acetate/hexane (1:10 v/v)

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05166213uspto-grants-1992_11