反应 #73508

ord-7d08a98027d6459dbd05d8c9c0b06277

反应方程式

C=C(c1ccccc1)C(C(C)=O)C(=O)OC
methyl 2-acetyl-3-phenylbut-3-enoate
C[CH2][Zn][CH2]C
diethylzinc
ICI
diiodomethane
O
water
COC(=O)C(C(C)=O)C1(c2ccccc2)CC1
methyl 3-oxo-2(1-phenylcyclopropyl)butanoate
收率 26.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction medium is refluxed for 18 hours
  2. 2
    萃取extracted with DCM (3×100 mL)
  3. 3
    洗涤washed successively with water (4×100 mL) and brine (100 mL)
  4. 4
    干燥dried over Na2SO4
  5. 5
    过滤filtered
  6. 6
    浓缩concentrated under reduced pressure
  7. 7
    其他The residue obtained
  8. 8
    其他is purified by chromatography on a column of silica gel
  9. 9
    洗涤eluting with a 95/5 cyclohexane/EtOAc mixture

实验过程

To a solution of 1 g (4.6 mmol) of methyl 2-acetyl-3-phenylbut-3-enoate in 16 mL of DCM are successively added dropwise 20.8 mL (22.9 mmol) of a 1.1M solution of diethylzinc in toluene and 3.7 mL (45.8 mmol) of diiodomethane. The reaction medium is refluxed for 18 hours. After cooling to room temperature, the reaction mixture is treated with 100 mL of water and then extracted with DCM (3×100 mL). The organic phases are combined, washed successively with water (4×100 mL) and brine (100 mL), dried over Na2SO4, filtered and then concentrated under reduced pressure. The residue obtained is purified by chromatography on a column of silica gel, eluting with a 95/5 cyclohexane/EtOAc mixture. 280 mg of methyl 3-oxo-2(1-phenylcyclopropyl)butanoate are obtained in the form of a yellow oil.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08541455B2uspto-grants-2013_09