反应 #2028872

ord-8728c19b691849d285beb6d3b7d1c141

反应方程式

Cl
HCl
COC(=O)C(=O)OC
Dimethyl oxalate
C[O-].[Na+]
sodium methoxide
CO
methanol
CC(=O)c1ccc(Cl)cc1
4′-chloroacetophenone
COC(=O)C(=O)CC(=O)c1ccc(Cl)cc1
yellow solid
收率 95.0%
COC(=O)C(=O)CC(=O)c1ccc(Cl)cc1
Methyl-4-[4-(chloro)phenyl]-2,4-dioxobutanoate
收率 95.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONadded to the reaction dropwise over 3 minutes
  2. 2
    workup.ADDITIONwere added
  3. 3
    其他The organic layer was collected
  4. 4
    洗涤washed with brine (350 mL)
  5. 5
    干燥dried over MgSO4
  6. 6
    过滤filtered
  7. 7
    浓缩concentrated in vacuo

实验过程

Dimethyl oxalate (23.6 g, 200 mmol) was placed in a 500 mL three-necked round bottom flask, and dissolved in diethyl ether (200 mL). To the stirred solution was added 25% sodium methoxide in methanol (48 mL, 210 mmol) via an addition funnel over a 2 minute period. Next, 4′-chloroacetophenone (25.94 g, 200 mmol) was dissolved in diethyl ether (50 mL), and added to the reaction dropwise over 3 minutes. After stirring overnight (18 hours), 1N HCl (400 mL) and ethyl acetate (750 mL) were added. The organic layer was collected, washed with brine (350 mL), dried over MgSO4, filtered, and concentrated in vacuo to give 45.7 g of a yellow solid. The solid was recrystallized from ethyl acetate and iso-octane to give 23 g (48%) of the dione: mp 108.5°-110.5° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE044048E1uspto-grants-2013_03