تفاعل #2028872

ord-8728c19b691849d285beb6d3b7d1c141

معادلة التفاعل

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
المردود 95.0%
COC(=O)C(=O)CC(=O)c1ccc(Cl)cc1
Methyl-4-[4-(chloro)phenyl]-2,4-dioxobutanoate
المردود 95.0%

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONadded to the reaction dropwise over 3 minutes
  2. 2
    workup.ADDITIONwere added
  3. 3
    أخرىThe organic layer was collected
  4. 4
    غسيلwashed with brine (350 mL)
  5. 5
    تجفيفdried over MgSO4
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated in vacuo

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE044048E1uspto-grants-2013_03