تفاعل #2286282
ord-5f22e7a4100847a0b6eb6f2dd78f20b0
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىat room temperature
- 2تركيزAt this time, the reaction mixture was concentrated under vacuum
- 3workup.ADDITIONThe resulting solid was diluted with water (200 mL)
- 4استخلاصextracted with ethyl acetate (200 mL)
- 5workup.ADDITIONThe water layer was acidified to pH=4 by the addition of a 1N aqueous hydrochloric acid solution
- 6استخلاصwas extracted with ethyl acetate (2×200 mL)
- 7غسيلwashed with a saturated aqueous sodium chloride solution
- 8تجفيفdried with magnesium sulfate
- 9ترشيحfiltered
- 10تركيزconcentrated under vacuum
- 11أخرىto afford a solid
- 12أخرىThe solid was dried overnight under high vacuum
الإجراء التجريبي
A solution of [4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester (8a) (1.66 g, 4.75 mmol, contains a minor amount of isomer) in methanol (50 mL) at room temperature was treated dropwise with a 1N aqueous sodium hydroxide solution (9.5 mL, 9.50 mmol). The reaction was stirred at room temperature for 24 h. At this time, the reaction mixture was concentrated under vacuum. The resulting solid was diluted with water (200 mL) and extracted with ethyl acetate (200 mL). The ethyl acetate layer was discarded. The water layer was acidified to pH=4 by the addition of a 1N aqueous hydrochloric acid solution and was extracted with ethyl acetate (2×200 mL). The organic layers were combined, washed with a saturated aqueous sodium chloride solution, dried with magnesium sulfate, filtered and concentrated under vacuum to afford a solid. The solid was dried overnight under high vacuum to afford [4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid (9a) (1.58 g, 100%, contains a minor amount of isomer) as an off-white solid; EI(+)-HRMS m/z calcd for C17H19ClN2O3 (M+) 334.1084, found 334.1083. Molecular Weight=334.8056; Exact Mass=334.1084