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Benzyl Chloride → Ethyl 2-(1-benzylpiperidin-4-yl)acetate

HRID 2379721
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HRID 2379721 반응식
[NH:1]1[CH2:6][CH2:5][CH:4]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:3][CH2:2]1.C(N(CC)CC)C.[CH2:20](Cl)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>C(Cl)Cl>[CH2:20]([N:1]1[CH2:6][CH2:5][CH:4]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:3][CH2:2]1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7503Benzyl ChlorideHCID 8471TriethylamineHCID 2760465Ethyl 2-(piperidin-4-yl)acetate

생성물 1

HCID 10400444Ethyl 2-(1-benzylpiperidin-4-yl)acetate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Ethyl 4-piperidylacetate was dissolved in 50 ml CH2Cl2 while chilling the mixture on an ice bath, 3.1 ml (22 mmol) triethylamine then benzyl chloride was added; the mixture was refluxed for 2 hours. After cooling the organic layer was extracted with water, brine and then dried over magnesium sulfate. After crystallization, 2.05 g of ethyl N-benzyl-4-piperidylacetate was obtained (Formula XI: Y'=CH2, alkyl=C2H5).

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후처리

  1. temperaturewhile chilling the mixture on an ice bath
  2. temperaturethe mixture was refluxed for 2 hours
  3. temperatureAfter cooling the organic layer
  4. extractionwas extracted with water, brine
  5. dry with materialdried over magnesium sulfate
  6. customAfter crystallization

출처 및 근거

ORD 기록
ord-87b5cd366eac4fb1a410afd0123cc0e8
출처 데이터셋
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05364865

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