تفاعل #437039
ord-ebaaf5367dca48d7972d39722dbce9fd
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىThe methanol was removed in vacuo
- 2workup.ADDITIONthe remaining solution was diluted with water (200 mL)
- 3استخلاصThe aqueous solution was extracted with ether (2×200 mL)
- 4استخلاصextracted again with ether (2×200 mL)
- 5غسيلThe combined organics were washed with brine (1×200 mL)
- 6تجفيفdried with magnesium sulfate
- 7تركيزconcentrated in vacuo
- 8أخرىThe while solid was dried overnight at 40° C. under vacuum
- 9أخرىIsolated yield: 4.3 g (95%)
الإجراء التجريبي
To a solution of methyl ester F4 (4.7 g, 16 mmol) in methanol (100 mL) was added a solution of LiOH (6.8 g, 160 mmol) in water (50 mL) and the solution was heated at 50° C. for 14 h. The methanol was removed in vacuo and the remaining solution was diluted with water (200 mL). The aqueous solution was extracted with ether (2×200 mL), acidified with 1N HCl (200 mL) and extracted again with ether (2×200 mL). The combined organics were washed with brine (1×200 mL), dried with magnesium sulfate and concentrated in vacuo. The while solid was dried overnight at 40° C. under vacuum. Isolated yield: 4.3 g (95%). 1H NMR (400 MHz, DMSO-d6): δ 12.95 (bs, 1H), 3.93 (s, 1H), 3.84–3.74 (m, 2H), 1.38 (s) +1.33 (s) (9H), 1.19 (s, 3H), 1.01 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −111.4 (dt, J=227, 13 Hz) +−112.4 (dt, J=227, 13 Hz) (1F), −113.5 (dt, J=227, 14 Hz) +−113.9 (dt, J=227, 15 Hz) (1F); MS-APCI (m/z+): 180.1, (m/z−): 278.