Реакция #434477

ord-96b3cf9eec9341c2a75d9f25788a4a8a

Уравнение реакции

OCCCCCCCCCCCCBr
12-bromododecanol
COc1ccc(CS)cc1
p-methoxybenzylmercaptan
C[O-]
methoxide
COc1ccc(CSCCCCCCCCCCCCO)cc1
pure product
Выход 90.0%
COc1ccc(CSCCCCCCCCCCCCO)cc1
12-p-methoxybenzylthio-1-dodecanol
Выход 90.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITAfter a few minutes
  2. 2
    ФильтрацияAfter a minimum of 3 h, the reaction was filtered
  3. 3
    Промывкаwashed 3× with cold MeOH

Методика

Na (800 mg, 34.8 mmol) was dissolved in 30 mL of dry MeOH. Under argon, p-methoxybenzylmercaptan (2.75 mL, 3.04 g, 19.7 mmol) was added to the methoxide solution. After a few minutes, 12-bromododecanol (2.5 g, 9.43 mmol) was dropped into the reaction mixture. Within 5 minutes a solid began to come out of solution. After a minimum of 3 h, the reaction was filtered and washed 3× with cold MeOH, yielding 2.874 g (8.49 mmol, 90%) of pure product after drying. 1H NMR (CDCl3): d 7.23 (d, J=8.8 Hz, 2H, AA′ of AA′ BB′ aromatic system), 6.85 (d, J=8.8 Hz, 2H, BB′ of AA′ BB′ aromatic system), 3.80 (s, 3H, methoxy), 3.66 (s, 2H, benzyl), 3.64 (dt, J1=6.6 Hz, J2=5.5 Hz, 2H, RCH2OH), 2.40 (t, J=7.3 Hz, 2H, RSCH2R), 1.50–1.65 (cm, 4H, CH2 b to heteroatoms), 1.2–1.4 (cm, 16H, bulk methylenes).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07173130B2uspto-grants-2007_02