تفاعل #2028866

ord-bd176ec4d79e4b9988e1efc93c640b21

معادلة التفاعل

Cl
HCl
CCOC(=O)C(F)(F)F
Ethyl trifluoroacetate
C[O-].[Na+]
sodium methoxide
CC(=O)c1ccc(Cl)cc1
4′-chloroacetophenone
O=C(CC(=O)C(F)(F)F)c1ccc(Cl)cc1
yellow-orange solid
المردود 93.3%
O=C(CC(=O)C(F)(F)F)c1ccc(Cl)cc1
4,4,4-trifluoro-1-[4-(chloro)phenyl]-butane-1,3-dione
المردود 93.3%

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONadded to the reaction dropwise over 5 minutes
  2. 2
    workup.ADDITIONwas added
  3. 3
    أخرىThe organic layer was collected
  4. 4
    غسيلwashed with brine (75 mL)
  5. 5
    تجفيفdried over MgSO4
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated in vacuo

الإجراء التجريبي

Ethyl trifluoroacetate (23.52 g, 166 mmol) was placed in a 500 mL three-necked round bottom flask, and dissolved in methyl tert-butyl ether (75 mL). To the stirred solution was added 25% sodium methoxide (40 mL, 177 mmol) via an addition funnel over a 2 minute period. Next 4′-chloroacetophenone (23.21 g, 150 mmol) was dissolved in methyl tert-butyl ether (20 mL), and added to the reaction dropwise over 5 minutes. After stirring overnight (15.75 hours), 3N HCl (70 mL) was added. The organic layer was collected, washed with brine (75 mL), dried over MgSO4, filtered, and concentrated in vacuo to give a 35.09 g of yellow-orange solid. The solid was recrystallized from iso-octane to give 31.96 g (85%) of the dione: mp66°-67° C.

المصدر

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