تفاعل #595342

ord-ef11e99b327e4ac294f0d0ac5f70c266

معادلة التفاعل

Cl
hydrogen chloride
CCC(=O)C(C)=NO
2,3-pentanedione 2-oxime
O=Cc1ccc(Cl)cc1
4-chlorobenzaldehyde
CC(=O)O
acetic acid
CCc1oc(-c2ccc(Cl)cc2)[n+]([O-])c1C
2-(4-Chlorophenyl)-5-ethyl-4-methyl-1,3-oxazole 3-oxide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONis then introduced for 30 min
  2. 2
    أخرىA precipitate is formed
  3. 3
    ترشيحwhich is filtered off with suction
  4. 4
    غسيلwashed twice with in each case 2 ml of diethyl ether
  5. 5
    استخلاصThe suspension is then extracted four times with in each case 10 ml of dichloromethane
  6. 6
    تجفيفThe combined organic phases are dried over magnesium sulfate
  7. 7
    أخرىthe solvent is removed on a rotary evaporator
  8. 8
    أخرىThe residue is used without further purification in the subsequent reaction

الإجراء التجريبي

1.00 g (8.69 mmol) of 2,3-pentanedione 2-oxime and 1.34 g (9.55 mmol) of 4-chlorobenzaldehyde are initially charged in 2 ml (34.94 mmol) of glacial acetic acid. With ice-cooling of the reaction mixture, hydrogen chloride gas is then introduced for 30 min. 10 ml of diethyl ether are then added to the reaction mixture. A precipitate is formed, which is filtered off with suction and washed twice with in each case 2 ml of diethyl ether. The precipitate is resuspended in about 5 ml of water, and the suspension is made basic using ammonia. The suspension is then extracted four times with in each case 10 ml of dichloromethane. The combined organic phases are dried over magnesium sulfate and the solvent is removed on a rotary evaporator. The residue is used without further purification in the subsequent reaction.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09095582B2uspto-grants-2015_08