تفاعل #79262

ord-b6f10bb60a1849a3805cb01a186bef25

الكواشف

لا شيء

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    workup.STIRRINGThe reaction was stirred at −78° C. for 30 minutes
  2. 2
    workup.STIRRINGstirred at −78° C. for 2 hr
  3. 3
    درجة الحرارةThe reaction mixture was warmed to rt
  4. 4
    ترشيحfiltered
  5. 5
    تجفيفThe filtrate was dried over MgSO4
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated to a residue
  8. 8
    أخرىThe residue was purified by flash column chromatography (Silica gel; Ethyl acetate/Hexane: 3/7)

الإجراء التجريبي

To a solution of TMEDA (6.6 mmol) in dry THF (15 mL), was added Sec-BuLi (6.6 mmol) slowly at −78° C. The reaction mixture was stirred at −78° C. for 10 minute, veratrole (6.0 mmol) in THF (3 mL) was added slowly. The reaction was stirred at −78° C. for 30 minutes, 1-chlorobutan-4-al (6.6 mmol) was added and stirred at −78° C. for 2 hr. The reaction mixture was warmed to rt, added brine (1 mL), and filtered. The filtrate was dried over MgSO4, filtered and concentrated to a residue. The residue was purified by flash column chromatography (Silica gel; Ethyl acetate/Hexane: 3/7) to afford 1-(2,3-dimethoxyphenyl)-4-chlorobutan-1-ol in 20% yield. 1H NMR (300 MHz, CDCl3) δ7.05 (dd, J=8.0 Hz, 7.7 Hz, 1H), 6.94 (bd, J=7.7 Hz, 1H), 6.85 (bd, J=8.1 Hz, 1H), 4.91-4.97 (m, 1H), 3.88 (s, 3H), 3.84 (s, 3H), 3.56-3.60 (m, 2H), 2.44-2.45 (m, 1H), 1.81-2.00 (m, 4H) ppm. MS (CI, NH3) m/e 244 (base, M+H+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06713471B1uspto-grants-2004_03