反応 #1771994

ord-4e7dee2502b84ab18ecf35021b18dcc9

反応方程式

CC1(C(=O)O)CCCCC1
1-methyl-1-hydroxycarbonylcyclohexane
B#B
diborane
CC1(CO)CCCCC1
1-methyl-1-hydroxymethylcyclohexane
収率 69.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The cooling bath was removed
  2. 2
    その他The remaining borane was quenched by the slow addition of saturated sodium bisulfate (10 mL) over 90 min
  3. 3
    温度with cooling
  4. 4
    workup.ADDITIONAdditional saturated sodium bisulfate (200 mL) was added and after 20 min
  5. 5
    workup.STIRRINGof stirring the aqueous layer
  6. 6
    その他was removed
  7. 7
    洗浄The organic layer was washed with water and saturated sodium chloride
  8. 8
    その他dried
  9. 9
    ろ過filtered
  10. 10
    濃縮concentrated
  11. 11
    その他The residue was purified by flash chromatography

実験手順

To a solution of 1-methyl-1-hydroxycarbonylcyclohexane (10 g, 70 mmol) in tetrahydrofuran(300 mL) at 0° C. was added 1M diborane in tetrahydrofuran (200 mL, 200 mmol) over 90 minutes. The cooling bath was removed and the reaction mixture was stirred at room temperature for two days. The remaining borane was quenched by the slow addition of saturated sodium bisulfate (10 mL) over 90 min with cooling. Additional saturated sodium bisulfate (200 mL) was added and after 20 min of stirring the aqueous layer was removed. The organic layer was washed with water and saturated sodium chloride, dried, filtered and concentrated. The residue was purified by flash chromatography using 20% diethylether in hexanes to give 1-methyl-1-hydroxymethylcyclohexane (6.17 g, 48 mmol, 69%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE043298E1uspto-grants-2012_04