Réaction #577205

Équation de réaction

3-((tosyloxy)methyl)-3-ethyloxetane

ethyl hydroxybiphenylcarboxylate

potassium hydroxide

ethanol

→

4-(3-ethyloxetane-3-ylmethoxy)biphenylcarboxylic acid

Rendement 51.7%

Solvants

toluene

Water

Conditions de réaction

Traitement

1. 1
   Autreto 45° C.
2. 2
   Températurerefluxed for 2 hours
3. 3
   Autrethe toluene layer was separated
4. 4
   LavageThe toluene layer was washed with 3% hydrochloric acid
5. 5
   workup.DISTILLATIONa saturated sodium carbonate solution and water, and then toluene was distilled off
6. 6
   workup.ADDITION20 g of sodium hydroxide, 500 mL of ethanol and 100 mL of water were added to the resulting residue
7. 7
   Températurerefluxed for 2 hours
8. 8
   AutreA residue obtained
9. 9
   workup.DISTILLATIONby distilling ethanol
10. 10
    Autreto obtain crystals
11. 11
    AutreThe crystals thus obtained
12. 12
    Filtrationby filtering
13. 13
    Autrewere recrystallized from ethanol

Mode opératoire

12 g of ethyl hydroxybiphenylcarboxylate and 15 g of potassium hydroxide were added to 100 mL of ethanol, and stirred at 60° C. for 1 hour. After decreasing the temperature to 45° C., 15 g of 3-((tosyloxy)methyl)-3-ethyloxetane was added dropwise thereto, and then refluxed for 2 hours. Water and toluene were added thereto, and the toluene layer was separated. The toluene layer was washed with 3% hydrochloric acid, a saturated sodium carbonate solution and water, and then toluene was distilled off. 20 g of sodium hydroxide, 500 mL of ethanol and 100 mL of water were added to the resulting residue, and refluxed for 2 hours. A residue obtained by distilling ethanol off was put in 300 mL of 5% hydrochloric acid to obtain crystals. The crystals thus obtained by filtering were recrystallized from ethanol to obtain 8 g of 4-(3-ethyloxetane-3-ylmethoxy)biphenylcarboxylic acid (OX2), which had a melting point of 222 to 225° C.

Source