反应 #52853

ord-1d3460c5657a46a1b80f064616bcbac3

反应方程式

CC(C)OB(OC(C)C)OC(C)C
triisopropylborate
CC1(C)CCCc2cc(Br)ccc21
6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene
[Li][CH2]CCC
n-BuLi
CC1(C)CCCc2cc(B(O)O)ccc21
title compound
CC1(C)CCCc2cc(B(O)O)ccc21
(5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic Acid

反应条件

温度
-78°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGthe reaction stirred at room temperature for 12 h
  2. 2
    萃取extracted with ether (2×)
  3. 3
    洗涤The combined organic layer was washed with brine
  4. 4
    干燥dried over MgSO4
  5. 5
    浓缩concentrated in vacuo
  6. 6
    其他to give an oil
  7. 7
    其他Recrystallization from hexane

实验过程

To a cold (−78° C.) solution of 2.02 g (8.4 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene in 11.0 mL of toluene, was added 4.6 g (6.8 mL, 10.9 mmol, 1.6 M in hexane) of n-BuLi. The resulting solution was stirred at −78° C. for 45 min. and then 2.40 g (3.0 mL, 12.7 mmol) of triisopropylborate was dropwise added and the reaction stirred at room temperature for 12 h. The reaction was then diluted with 10% HCl, and extracted with ether (2×). The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Recrystallization from hexane afforded the title compound as a white solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06855832B2uspto-grants-2005_02