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1-Iodopropane → (Rac)-2-cyclopentylaminomethyl-pentanoic acid ethyl ester

HRID 2111259
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2111259
[CH2:1]([O:3][C:4](=[O:13])[CH2:5][CH2:6][NH:7][CH:8]1[CH2:12][CH2:11][CH2:10][CH2:9]1)[CH3:2].C[Si]([N-][Si](C)(C)C)(C)C.[Li+].I[CH2:25][CH2:26][CH3:27]>O1CCCC1>[CH2:1]([O:3][C:4](=[O:13])[CH:5]([CH2:6][NH:7][CH:8]1[CH2:12][CH2:11][CH2:10][CH2:9]1)[CH2:25][CH2:26][CH3:27])[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 336431-IodopropaneHCID 2733832Lithium hexamethyldisilazaneHCID 23053028Ethyl 3-(cyclopentylamino)propanoate

Produkt 1

HCID 57635032(Rac)-2-cyclopentylaminomethyl-pentanoic acid ethyl esterAusbeute 48,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a mixture of 2.0 g (0.0108 mole) of 3-cyclopentylamino-propanoic acid ethyl ester and 10 mL of anhydrous tetrahydrofuran, at −78 degrees, was added 24.0 mL (0.0236 mole) of lithium bis(trimethylsilyl)amide. The mixture was stirred for 1 hour and then a solution of 2.0 g (0.0119 mole) of iodopropane in 2.0 mL of tetrahydrofuran was added slowly. The mixture was stirred at room temperature for 24 hours and then quenched by the addition of water. The mixture was concentrated under reduced pressure and then extracted three times with 50 mL of ethyl acetate. The combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 1.2 g of (rac)-2-cyclopentylaminomethyl-pentanoic acid ethyl ester, which was used without further purification in subsequent steps.

Aufarbeitung

  1. stirringThe mixture was stirred at room temperature for 24 hours
  2. customquenched by the addition of water
  3. concentrationThe mixture was concentrated under reduced pressure
  4. extractionextracted three times with 50 mL of ethyl acetate
  5. dry with materialThe combined extracts were dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-a1cd2d3b2b4c4bef99b253234cb7ce22
Quelldatensatz
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07517873B2

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