Reaktion #312489

ord-957556a4e4754128af0b0e99c6d2da60

Reaktionsgleichung

C=O
formaldehyde
C=O
formalin
O=C(O)Cc1ccc(O)cc1
4-Hydroxybenzeneacetic acid
Cl
hydrochloric acid
O=C(O)Cc1ccc(O)c(CCl)c1
title compound
O=C(O)Cc1ccc(O)c(CCl)c1
3-Chloromethyl-4-hydroxybenzeneacetic acid

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeHydrogen chloride is bubbled through the reaction mixture for 60 minutes
  2. 2
    Temperaturwhile maintaining the temperature of the reaction mixture at 35° to 45° C
  3. 3
    workup.ADDITIONThe reaction mixture is poured into water
  4. 4
    Extraktionthe title compound is extracted from the solution with ethyl acetate
  5. 5
    TrocknenThe ethyl acetate is dried over magnesium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Sonstigeremoved

Vorschrift

4-Hydroxybenzeneacetic acid, 0.5 mole, is added to concentrated hydrochloric acid, 50 ml, then 0.5 mole of formaldehyde in the form of a 34-38% solution of formalin is added. Hydrogen chloride is bubbled through the reaction mixture for 60 minutes while maintaining the temperature of the reaction mixture at 35° to 45° C. The reaction mixture is poured into water and the title compound is extracted from the solution with ethyl acetate. The ethyl acetate is dried over magnesium sulfate, filtered and removed to give the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04236002uspto-grants-1980_11