Реакция #947711

ord-847c5390e37340c1bc2d0ba46ef50d6b

Уравнение реакции

CCOC(=O)c1ccc2cc(Br)ccc2c1
ethyl 6-bromo-2-naphthoate
CC(C)[CH2][AlH][CH2]C(C)C
DIBAL
OCc1ccc2cc(Br)ccc2c1
6-bromo-2-naphthylmethyl alcohol
Выход 111.9%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter 1 hour the reaction mixture was quenched with ethyl acetate
  2. 2
    workup.ADDITIONThe mixture was diluted with ethyl acetate
  3. 3
    Промывкаwashed with 1.0 N HCl, water and brine
  4. 4
    СушкаThe organics were dried with magnesium sulfate
  5. 5
    Фильтрацияfiltered
  6. 6
    Другоеevaporated

Методика

To a solution of ethyl 6-bromo-2-naphthoate (7.90 g, 28.30 mmol) in 200 mL toluene at −78° C. under an atmosphere of argon was added DIBAL (84.9 mL, 1.0 M in toluene, 84.91 mmol) via transfer needle over 20 minutes. After 1 hour the reaction mixture was quenched with ethyl acetate and the resulting mixture was allowed to warm to RT. The mixture was diluted with ethyl acetate and washed with 1.0 N HCl, water and brine. The organics were dried with magnesium sulfate, filtered and evaporated to give 7.51 g of 6-bromo-2-naphthylmethyl alcohol as a white solid and used without further purification in the oxidation (step c). 1H NMR (300 MHz; CDCl3): δ 4.86 (s, 2H); 7.50 (dd, J1=2.0 Hz, J2=8.0 Hz, 1H); 7.57 (d, J=2.0 Hz, 1H); 7.70 (d, J=9.0 Hz, 1H); 7.75 (d, J=8.0 Hz, 1H); 7.79 (s, 1H); 8.00 (d, J=2.0 Hz, 1H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07153875B2uspto-grants-2006_12