Reaktion #349578

ord-37b182d5d2eb41d79c8e5f2a89c4a45a

Reaktionsgleichung

Cl
hydrochloric acid
O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO
D-(+)-galactose
CCCCCCCCCCCCOS(=O)(=O)c1ccccc1.[Na]
sodium laurylbenzenesulfonate
Cl
hydrogen chloride
Cc1ccccc1
toluene
O=Cc1ccc(CCl)o1
5-chloromethylfurfural

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGat 50° C. over 3 hours with stirring
  2. 2
    workup.STIRRINGAfter stirring
  3. 3
    Filtrationfiltered through Celite
  4. 4
    Waschenwhile being washed with toluene
  5. 5
    Sonstigedried
  6. 6
    Einengenconcentrated

Vorschrift

To the same three-necked flask as in Example 1 were added 5 g (0.028 mole) of a commercially available D-(+)-galactose and two kinds of surface active agent, i.e., 89.6 mg (0.00028 mole) of cetyltrimethylammonium chloride and 97.6 mg (0.00028 mole) of sodium laurylbenzenesulfonate. Then, 30 ml of toluene was added thereto and the mixture was stirred to make a suspension. Thereafter, about 6 ml of 35% aqueous hydrochloric acid was added dropwise from a dropping funnel over about 1 hour. A slight excess of hydrogen chloride was then slowly passed therethrough at 50° C. over 3 hours with stirring. After stirring was continued for a further 5 hours, the reaction solution was diluted with a little water and filtered through Celite while being washed with toluene. The toluene layer was neutralized, dried and concentrated to obtain about 1.9 g (theoretical yield 4.01 g) of 5-chloromethylfurfural as a crude product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04154744uspto-grants-1979_05