تفاعل #969892

ord-697c2977aeb04bf8b9cec086140eedc9

معادلة التفاعل

Cl
hydrochloric acid
CCOC(=O)C(C)(C)Br
ethyl 2-bromoisobutyrate
NC1C2CC3CC(C2)CC1C3
2-adamantylamine
O=Cc1ccccc1
benzaldehyde
CC1(C)C(=O)N(C2C3CC4CC(C3)CC2C4)C1c1ccccc1
1-(adamantan-2-yl)-3,3-dimethyl-4-phenylazetidin-2-one
المردود 64.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe reaction solution was concentrated in vacuo
  2. 2
    workup.DISSOLUTIONThe obtained residue was dissolved in toluene (5 mL)
  3. 3
    workup.STIRRINGThe reaction solution was stirred at 130° C. for 5 hours
  4. 4
    استخلاصextracted with ethyl acetate
  5. 5
    تجفيفThe organic layer was dried with anhydrous sodium sulfate
  6. 6
    تركيزconcentrated in vacuo
  7. 7
    أخرىThe obtained residue was purified

الإجراء التجريبي

A solution of 2-adamantylamine (50.0 mg, 0.330 mmol) in ethanol (2 mL) was added with benzaldehyde (56.3 mg, 0.330 mmol) at room temperature, and the resultant was stirred at the same temperature for 1.5 hours. The reaction solution was concentrated in vacuo. The obtained residue was dissolved in toluene (5 mL), and sequentially added with ethyl 2-bromoisobutyrate (109 mg, 0.660 mmol) and zinc (432 mg, 6.60 mmol) at room temperature. The reaction solution was stirred at 130° C. for 5 hours, and added with hydrochloric acid, and extracted with ethyl acetate. The organic layer was dried with anhydrous sodium sulfate, and concentrated in vacuo. The obtained residue was purified using preparative thin-layer chromatography (hexane:ethyl acetate=3:1), and 1-(adamantan-2-yl)-3,3-dimethyl-4-phenylazetidin-2-one (65.4 mg, 64.0%) was obtained as a white crystalline powder.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08236789B2uspto-grants-2012_08