反应 #1755468

ord-3ab14c3c8f0747a1963d72b118515d20

反应方程式

C#CCC1CCC(CO)CC1
86
C#CCC1CCC(CO)CC1
(4-Prop-2-ynyl-cyclohexyl)-methanol
c1ccncc1
pyridine
CC(=O)OC(C)=O
acetic anhydride
C#CCC1CCC(COC(C)=O)CC1
87
收率 91.4%
C#CCC1CCC(COC(C)=O)CC1
(4-prop-2-ynylcyclohexyl)methyl acetate
收率 91.4%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.WAITAfter 16 hours
  2. 2
    温度The reaction mixture was heated at 75° C. for 3 hours
  3. 3
    其他The solvent was removed under reduced pressure
  4. 4
    其他to yield a yellow oil which
  5. 5
    其他was purified by flash chromatography, on silica gel
  6. 6
    洗涤eluting with 1:3 ether/petroleum ether

实验过程

To a solution of 960 mg (6.31 mmol) of 86 in 6 mL DMF was added 0.62 mL (7.57 mmol) pyridine and 0.78 mL (8.27 mmol) acetic anhydride. The reaction was allowed to stir overnight at room temperature. After 16 hours, starting material still remained. The reaction mixture was heated at 75° C. for 3 hours. The solvent was removed under reduced pressure to yield a yellow oil which was purified by flash chromatography, on silica gel, eluting with 1:3 ether/petroleum ether to yield 1.12 g (91%) of 87 as an oil. 1H NMR (CDCl3) δ3.87 (d, J=6.2 Hz, 2H), 2.06 (d, J=4.3 Hz, 2H), 2.03 (s, 3H), 1.98-1.93 (m, 1H), 1.92-1.83 (m, 2H), 1.83-1.74 (m, 2H), 1.63-1.36 (m, 2H), 1.12-0.90 (m, 4H); 13C NMR (CDCl3) δ 171.7, 83.7, 69.9, 69.6, 37.4, 37.3, 32.1, 29.7, 26.5, 21.4; APCI m/z (rel intensity) 195 (M+, 30), 153 (M+, 70), 135 (M+, 100).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07989431B2uspto-grants-2011_08