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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Anhydride → 1-(3-Hydroxypiperidin-1-yl)ethan-1-one

HRID 355123
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인쇄 미리보기

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HRID 355123 반응식
[OH:1][CH:2]1[CH2:7][CH2:6][CH2:5][NH:4][CH2:3]1.[C:8](OC(=O)C)(=[O:10])[CH3:9]>C(Cl)Cl>[C:8]([N:4]1[CH2:5][CH2:6][CH2:7][CH:2]([OH:1])[CH2:3]1)(=[O:10])[CH3:9]
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참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 232933-Hydroxypiperidine

생성물 1

HCID 218970301-(3-Hydroxypiperidin-1-yl)ethan-1-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
10 °C

실험 절차

3-Hydroxypiperidine (0.4 mole) is dissolved in 150 ml. of methylene chloride. The solution is cooled to 10° C. and acetic anhydride (0.46 mole) is added dropwise, maintaining the temperature under 20° C. The reaction mixture is allowed to come to room temperature, and is then refluxed for 2 hours. The methylene chloride is evaporated off, and the remaining liquid is distilled under high vacuum. A thick yellow oil is collected at 122°-126° C. (0.3 mm Hg).

후처리

  1. temperaturemaintaining the temperature under 20° C
  2. customto come to room temperature
  3. temperatureis then refluxed for 2 hours
  4. customThe methylene chloride is evaporated off
  5. distillationthe remaining liquid is distilled under high vacuum
  6. customA thick yellow oil is collected at 122°-126° C. (0.3 mm Hg)

출처 및 근거

ORD 기록
ord-0b73d369403e428bad7718ae4e2f4d7f
출처 데이터셋
uspto-grants-1983_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04377521

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