Réaction #59776

Équation de réaction

2-hydroxy-5-bromo-phenylacetic acid

potassium tert.butoxide

benzylbromide

→

2-benzyloxy-5-bromo-phenylacetic acid

Solvants

dimethylformamide

Conditions de réaction

Traitement

1. 1
   workup.ADDITIONpoured onto ice water
2. 2
   Extractionextracted with ethyl acetate
3. 3
   AutreThe combined organic extracts are dried
4. 4
   Autreevaporated down
5. 5
   workup.DISSOLUTIONThe residue is dissolved in 100 ml of ethanol
6. 6
   workup.ADDITIONafter the addition of 50 ml of 2N sodium hydroxide solution
7. 7
   workup.STIRRINGstirred for 3 hours at ambient temperature
8. 8
   workup.DISTILLATIONThe solvent is distilled off
9. 9
   ExtractionAfter extraction with ethyl acetate the organic phases
10. 10
    Autreare dried
11. 11
    Autreevaporated down
12. 12
    AutreThe residue is chromatographed on silica gel
13. 13
    Lavageeluted with petroleum ether/ethyl acetate (8:2)

Mode opératoire

A solution of 12.4 g (0.053 mol) of 2-hydroxy-5-bromo-phenylacetic acid in 125 ml of dimethylformamide is combined with 14 g (0.125 mol) of potassium tert.butoxide. After 15 minutes at ambient temperature 18.5 g (0.108 mol) of benzylbromide are added. The reaction solution is stirred for 3 hours at ambient temperature, poured onto ice water and extracted with ethyl acetate. The combined organic extracts are dried and evaporated down. The residue is dissolved in 100 ml of ethanol and after the addition of 50 ml of 2N sodium hydroxide solution stirred for 3 hours at ambient temperature. The solvent is distilled off, the residue is adjusted to pH 4 with 2N hydrochloric acid. After extraction with ethyl acetate the organic phases are dried and evaporated down. The residue is chromatographed on silica gel and eluted with petroleum ether/ethyl acetate (8:2).

Source