Benzene → 1,3-Dioxolane, 2-(bromomethyl)-2-(2-naphthalenyl)-

HRID 1679128

Reaktionsgleichung

Reaktionsgleichung von HRID 1679128
[Br:1][CH2:2][C:3]([C:5]1[CH:14]=[CH:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=1)=[O:4].[CH2:15]([OH:19])[CH2:16]CC.CC1C=CC(S(O)(=O)=O)=CC=1.C1C=CC=CC=1>C(O)CO>[Br:1][CH2:2][C:3]1([C:5]2[CH:14]=[CH:13][C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[CH:6]=2)[O:19][CH2:15][CH2:16][O:4]1

Komponenten

6

Versuchsvorschrift

To a stirred solution of 74.4 parts of 2-bromo-1-(2-naphthalenyl)-1-ethanone in 240 parts of a butanol are added successively 3 parts of 4-methylbenzenesulfonic acid and 270 parts of benzene. Then there are added dropwise 28 parts of 1,2-ethanediol. Upon completion, stirring is continued overnight at reflux temperature. The reaction mixture is evaporated. The residue is dissolved in 2,2'-oxybispropane and the solution is stirred with a diluted sodium hydroxide solution. The layers are separated and the aqueous phase is extracted with 2,2'-oxybispropane. The extra ct is neutralized with water, dried, filtered and evaporated. The oily residue is crystallized from methanol. The product is filtered off and recrystallized from methanol, yielding 41 parts of 2-(bromomethyl)-2-(2-naphthalenyl)-1,3-dioxolane; mp. 64° C.

Aufarbeitung

  1. temperatureat reflux temperature
  2. customThe reaction mixture is evaporated
  3. dissolutionThe residue is dissolved in 2,2'-oxybispropane
  4. stirringthe solution is stirred with a diluted sodium hydroxide solution
  5. customThe layers are separated
  6. extractionthe aqueous phase is extracted with 2,2'-oxybispropane
  7. customdried
  8. filtrationfiltered
  9. customevaporated
  10. customThe oily residue is crystallized from methanol
  11. filtrationThe product is filtered off
  12. customrecrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-4c3488e9e9b24c9492349b3290d13e59
Quelldatensatz
uspto-grants-1978_03
Patentnummer
US04079062

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