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Dimethylformamide → 1-Acetyl-3-benzyloxypiperidine

HRID 355124
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반응식

HRID 355124 반응식
[C:1]([N:4]1[CH2:9][CH2:8][CH2:7][CH:6]([OH:10])[CH2:5]1)(=[O:3])[CH3:2].CN(C)C=O.[H-].[Na+].[CH2:18](Cl)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>O>[C:1]([N:4]1[CH2:9][CH2:8][CH2:7][CH:6]([O:10][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:5]1)(=[O:3])[CH3:2]
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참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 7503Benzyl ChlorideHCID 24758Sodium hydrideHCID 218970301-(3-Hydroxypiperidin-1-yl)ethan-1-one

생성물 1

HCID 205061191-Acetyl-3-benzyloxypiperidine

시약·촉매·용매 1

HCID 962Water용매

실험 절차

1-Acetyl-3-hydroxypiperidine (0.10 mole) is dissolved in 50 ml. of dimethylformamide. 0.12 Mole of sodium hydride (56%) is added over a 10 minute period, and the reaction mixture is stirred for 30 minutes. Benzyl chloride (0.12 mole) is added dropwise over a 30 minute period, and the reaction mixture is then heated on a steam bath for 30 minutes. Water (3 volumes) is added, the solution extracted with ether, the ether extract washed with water and the ether removed by evaporation. A yellow oil is obtained on distillation at 136°-140° C. (0.01 mm Hg.).

후처리

  1. temperaturethe reaction mixture is then heated on a steam bath for 30 minutes
  2. extractionthe solution extracted with ether
  3. extractionthe ether extract
  4. washwashed with water
  5. customthe ether removed by evaporation
  6. customA yellow oil is obtained on distillation at 136°-140° C. (0.01 mm Hg.)

출처 및 근거

ORD 기록
ord-290ac57bed404a7dac0e126a88c6a994
출처 데이터셋
uspto-grants-1983_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04377521

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