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o-Xylyl bromide → N-(2-methylbenzyl)4-piperidone

HRID 1179329
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HRID 1179329 반응식
Cl.O.[NH:3]1[CH2:8][CH2:7][C:6](=[O:9])[CH2:5][CH2:4]1.C(=O)([O-])[O-].[K+].[K+].[CH3:16][C:17]1[CH:24]=[CH:23][CH:22]=[CH:21][C:18]=1[CH2:19]Br>CC#N>[CH3:16][C:17]1[CH:24]=[CH:23][CH:22]=[CH:21][C:18]=1[CH2:19][N:3]1[CH2:8][CH2:7][C:6](=[O:9])[CH2:5][CH2:4]1
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참가 물질

5

반응물 3

HCID 6992o-Xylyl bromideHCID 11430Potassium CarbonateHCID 2723901Piperonylamine

생성물 1

HCID 11959536N-(2-methylbenzyl)4-piperidone

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
0 °C

실험 절차

To a suspension of 2.00 g of 4-piperidone monohydrate hydrochloride and 5.40 g of potassium carbonate in 30 ml of CH3CN was added dropwise 1.57 ml of 2-methyl benzyl bromide at 0° C. After stirred at 0° C. or 3.5 h, the mixture was stirred at room temperature for an hour. At 0° C., the mixture was quenched with water and extracted with CHCl3. The organic layer was washed with water, aqueous NaOH, and brine, and dried over anhydrous Na2SO4. The organic solvent was evaporated to give the crude product of 2.52 g of N-(2-methylbenzyl)-4-piperidone as a yellow oil.

후처리

  1. stirringthe mixture was stirred at room temperature for an hour
  2. customAt 0° C., the mixture was quenched with water
  3. extractionextracted with CHCl3
  4. washThe organic layer was washed with water, aqueous NaOH, and brine
  5. dry with materialdried over anhydrous Na2SO4
  6. customThe organic solvent was evaporated

출처 및 근거

ORD 기록
ord-26b9fb9c1a1f408b8fd40ab93358bda6
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07279490B2

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