Reaktion #58889

ord-12868647474649d7a47cf0fd64862070

Reaktionsgleichung

Cc1ccccc1-c1ccc(O)c(C=O)c1
4-hydroxy-2′-methyl-biphenyl-3-carbaldehyde
OCCCO
1,3-dihydroxypropane
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
Cc1ccccc1-c1ccc(O)c(C2OCCCO2)c1
title product
Ausbeute 89.0%
Cc1ccccc1-c1ccc(O)c(C2OCCCO2)c1
3-[1,3]Dioxan-2-yl-2′-methyl-biphenyl-4-ol
Ausbeute 89.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheated
  2. 2
    Temperaturat reflux overnight in a Dean-Stark
  3. 3
    TemperaturThe reaction was cooled
  4. 4
    Waschenwashed with a solution of Na2CO3 (aq, 1 M)
  5. 5
    SonstigeEvaporation in vacuo

Vorschrift

A solution of 4-hydroxy-2′-methyl-biphenyl-3-carbaldehyde (18.8 mmol) in toluene (100 mL) was added 1,3-dihydroxypropane (65.7 mmol) and p-toluenesulfonic acid (cat) and heated at reflux overnight in a Dean-Stark set-up. The reaction was cooled and washed with a solution of Na2CO3 (aq, 1 M). Evaporation in vacuo gave the title product as brown oil in 89% yield. 1H-NMR (CDCl3) δ 9.61 (bs, 1H), 7.34-7.10 (m, 6H), 6.87 (d, 1H), 5.77 (s,1H), 4.13-4.07 (m, 2H), 3.95-3.86 (m, 2H), 2.20 (s, 3H), 2.18-1.96 (m, 1H), 1.40 (d, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07423181B2uspto-grants-2008_09