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Triethylamine → 1-(Methanesulfonyl)piperidin-3-ol

HRID 456444
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HRID 456444 반응식
[NH:1]1[CH2:6][CH2:5][CH2:4][CH:3]([OH:7])[CH2:2]1.C(N(CC)CC)C.[CH3:15][S:16](Cl)(=[O:18])=[O:17]>C1COCC1.C(Cl)Cl.C(OCC)(=O)C>[CH3:15][S:16]([N:1]1[CH2:6][CH2:5][CH2:4][CH:3]([OH:7])[CH2:2]1)(=[O:18])=[O:17]
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참가 물질

6

반응물 3

HCID 8471TriethylamineHCID 232933-HydroxypiperidineHCID 31297Methanesulfonyl chloride

생성물 1

HCID 179180311-(Methanesulfonyl)piperidin-3-ol

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 21919333Tetrahydrofurane dichloromethane용매

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온도
0 °C

실험 절차

Piperidin-3-ol (5.0 g, 49.4 mmol) was dissolved in 1/1 THF/methylene chloride (100 mL). Triethylamine (17 mL, 123 mmol) was added, and the solution was cooled to 0° C. Methanesulfonyl chloride (4.0 mL, 52 mmol) was added dropwise. The mixture was warmed to r.t. and stirred overnight. The reaction was diluted with ethyl acetate (800 mL), washed with 1 N HCl (100 mL), water (75 mL), saturated aqueous sodium bicarbonate (75 mL) and brine (75 mL), and then dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure and purified via silica gel chromatography (ethyl acetate) to afford the title compound as a clear oil.

후처리

  1. temperatureThe mixture was warmed to r.t.
  2. washwashed with 1 N HCl (100 mL), water (75 mL), saturated aqueous sodium bicarbonate (75 mL) and brine (75 mL)
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationThe solvent was concentrated under reduced pressure
  5. custompurified via silica gel chromatography (ethyl acetate)

출처 및 근거

ORD 기록
ord-e02860db1c6e4a3aad97a78666f101b2
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07186715B2

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