تفاعل #81495

ord-e264f97dc01f4627802db2c89be88394

معادلة التفاعل

C1CO1
ethylene oxide
Cc1cccc(F)n1
2-fluoro-6-methylpyridine
C1CCOC1
THF
CC(C)[N-]C(C)C.[Li+]
LDA
OCCCc1cccc(F)n1
2-fluoro-6-(3-hydroxypropyl)pyridine
المردود 30.9%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto warm to room temperature
  2. 2
    workup.STIRRINGwith stirring
  3. 3
    استخلاصextracted with ether
  4. 4
    غسيلthe organic layer was washed with water (2x) and brine
  5. 5
    تجفيفdried over sodium sulfate
  6. 6
    تركيزThe organic solution was concentrated
  7. 7
    أخرىthe residue was purified by flash chromatography (chloroform/ethanol, 10:1)

الإجراء التجريبي

To a solution of 2-fluoro-6-methylpyridine (27 mmol) in 65 ml of freshly distilled THF was added via syringe 13.5 ml of 2M LDA, and the resulting mixture was stirred at -78° C. for 20 min. To the above cold solution was added 4 ml of 4M ethylene oxide and the mixture was allowed to warm to room temperature with stirring. The mixture was diluted with water, extracted with ether, and the organic layer was washed with water (2x) and brine, and dried over sodium sulfate. The organic solution was concentrated, and the residue was purified by flash chromatography (chloroform/ethanol, 10:1) to yield 1.3 g (30.9%) of 2-fluoro-6-(3-hydroxypropyl)pyridine, as a yellow oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05618821uspto-grants-1997_04