反応 #577204
ord-20816e1ca3a541569af71e18a76e335f
反応方程式
反応条件
後処理
- 1その他to 45° C.
- 2workup.STIRRINGstirred at 45° C. for 3 hours
- 3その他the toluene layer was separated
- 4洗浄The toluene layer was washed with 3% hydrochloric acid
- 5workup.DISTILLATIONa saturated sodium carbonate solution and water, and then toluene was distilled off
- 6workup.ADDITION50 g of sodium hydroxide, 500 mL of ethanol and 200 mL of water were added to the resulting residue
- 7温度refluxed for 2 hours
- 8その他A residue obtained
- 9workup.DISTILLATIONby distilling ethanol
- 10その他to obtain crystals
- 11その他The crystals thus obtained
- 12ろ過by filtering
- 13その他were recrystallized from a mixed solvent of ethanol and water
実験手順
50 g of ethyl hydroxybenzoate and 21 g of potassium hydroxide were added to 400 mL of dimethylformamide, and stirred at 70° C. for 1 hour. After decreasing the temperature to 45° C., 100 g of 3-((tosyloxy)methyl)-3-ethyloxetane was added dropwise thereto, and then stirred at 45° C. for 3 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. 50 g of sodium hydroxide, 500 mL of ethanol and 200 mL of water were added to the resulting residue, and refluxed for 2 hours. A residue obtained by distilling ethanol off was put in 500 mL of 5% hydrochloric acid to obtain crystals. The crystals thus obtained by filtering were recrystallized from a mixed solvent of ethanol and water to obtain 60 g of 4-(3-ethyloxetane-3-ylmethoxy)benzoic acid (OX1), which had a melting point of 127.5° C.