تفاعل #484787

ord-f5102503fe3a4a0fb04bc62843922f07

معادلة التفاعل

C.ClC(c1ccccc1)(c1ccccc1)c1ccccc1
chlorotriphenylmethane methane
Cl.O.O=C1CCNCC1
4-piperidone monohydrate hydrochloride
CCN(CC)CC
triethylamine
O=C1CCN(C(c2ccccc2)(c2ccccc2)c2ccccc2)CC1
1-triphenylmethyl-4-piperidone
المردود 103.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe resulting mixture was stirring further for 5 hours at the same temperature
  2. 2
    أخرىThe triethylamine hydrochloride precipitated
  3. 3
    درجة الحرارةby cooling
  4. 4
    ترشيحwas filtered out
  5. 5
    تركيزthe filtrate was concentrated under reduced pressure
  6. 6
    workup.ADDITIONTo the residue was added 150 ml of water
  7. 7
    استخلاصfollowed by extraction with 300 ml of ethyl acetate
  8. 8
    غسيلThe organic layer was then washed with saturated saline
  9. 9
    تجفيفdried over anhydrous magnesium sulfate
  10. 10
    تركيزThe solvent was concentrated under reduced pressure

الإجراء التجريبي

After the portionwise addition of 18.1 g (65.1 mmol) of chlorotriphenylmethane methane to a 150 ml dimethylformamide solution of 10.0 g (65.1 mmol) of 4-piperidone monohydrate hydrochloride and 20.0 g (198 mmol) of triethylamine at 60° C. under stirring, the resulting mixture was stirring further for 5 hours at the same temperature. The triethylamine hydrochloride precipitated by cooling was filtered out and the filtrate was concentrated under reduced pressure. To the residue was added 150 ml of water, followed by extraction with 300 ml of ethyl acetate. The organic layer was then washed with saturated saline and dried over anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure, whereby 23.0 g (yield: 98.3%) of 1-triphenylmethyl-4-piperidone were obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06610708B1uspto-grants-2003_08