تفاعل #7255

ord-a94a42113b9747d29ec261a62954dea4

معادلة التفاعل

CN(C)C=O
DMF
CN(C)CCN(C)C
TMEDA
[Li][CH2]CCC
n-butyl lithium
Fc1cccnc1
3-fluoropyridine
O=Cc1ccncc1F
title compound
المردود 37.3%
O=Cc1ccncc1F
3-fluoro-pyridine-4-carboxaldehyde
المردود 37.3%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITAfter another 2 hours at −78° C.
  2. 2
    workup.WAITAfter a further 2 hours at −78° C.
  3. 3
    أخرىthe reaction was quenched with saturated aqueous NaHCO3 (20 mL)
  4. 4
    استخلاصextracted with ether (4×15 mL)
  5. 5
    تجفيفdried (Na2SO4)
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىto give the crude oil
  9. 9
    أخرىPurification by column chromatography on silica gel (Hexanes: EtOAc 4:1)

الإجراء التجريبي

To a solution of TMEDA (389 uL, 2.58 mmol) in THF (10 mL) at −78° C. was added a solution of n-butyl lithium in THF (2.5M, 1.03 mL, 2.58 mmol). After 30 minutes at −78° C., 3-fluoropyridine (221 uL, 2.57 mmol) was added. After another 2 hours at −78° C., DMF (219 uL, 2.83 mmol) was added. After a further 2 hours at −78° C., the reaction was quenched with saturated aqueous NaHCO3 (20 mL), extracted with ether (4×15 mL), dried (Na2SO4), filtered and concentrated in vacuo to give the crude oil. Purification by column chromatography on silica gel (Hexanes: EtOAc 4:1) afforded the title compound as a pale yellow oil (120 mg, 37%). 1H NMR (CDCl3) 7.68 (t, 1H, J=5.2 Hz), 8.62 (d, 1H, J=4.7 Hz), 8.70 (s, 1H), 10.42 (s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07084155B2uspto-grants-2006_08