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Water → 4-(3-Hydroxypropyloxymethyl)piperidine

HRID 1282003
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1282003
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][OH:15])[CH2:10][CH2:9]1)=O)(C)(C)C.Br[CH2:17][CH2:18][CH2:19][O:20][Si](C(C)C)(C(C)C)C(C)C.[H-].[Na+].O>CN(C=O)C>[OH:20][CH2:19][CH2:18][CH2:17][O:15][CH2:14][CH:11]1[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1
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Komponenten

6

Edukt 4

HCID 962WaterHCID 24758Sodium hydrideHCID 2764081Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 23510097(3-Bromopropoxy)tri(propan-2-yl)silane

Produkt 1

HCID 184234304-(3-Hydroxypropyloxymethyl)piperidine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

To a solution of 0.5 g (2.3 mmol) of 1-t-butoxycarbonyl-4-hydroxymethylpiperidine and 1.4 g (4.6 mmol) of 1-bromo-3-(triisopropylsilyloxy)propane in 3 mL of DMF was added 0.12 g (4.1 mmol) of NaH (60% dispersion in mineral oil) and the reaction mixture was stirred at rt for 16 h. To the reaction mixture was added 10 mL of H2O and it was extracted with ether. The combined organic fractions were washed with sat'd NaCl solution, dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes:ethyl acetate=19:1) to give the title compound.

Aufarbeitung

  1. extractionwas extracted with ether
  2. washThe combined organic fractions were washed with sat'd NaCl solution
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated
  6. customThe residue was purified by chromatography (silica, hexanes:ethyl acetate=19:1)

Quellen und Nachweise

ORD-Eintrag
ord-f4db2b8ac2b04ccd97831f461433e027
Quelldatensatz
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06455548B2

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