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Cesium carbonate → Tert-butyl 4-(3-(diethoxyphosphoryl)propoxy)phenethylcarbamate

HRID 2407892
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2407892
[OH:1][C:2]1[CH:17]=[CH:16][C:5]([CH2:6][CH2:7][NH:8][C:9](=[O:15])[O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[Cs+].[Cs+].Br[CH2:25][CH2:26][CH2:27][P:28](=[O:35])([O:32][CH2:33][CH3:34])[O:29][CH2:30][CH3:31]>CN(C=O)C>[CH2:33]([O:32][P:28]([CH2:27][CH2:26][CH2:25][O:1][C:2]1[CH:17]=[CH:16][C:5]([CH2:6][CH2:7][NH:8][C:9](=[O:15])[O:10][C:11]([CH3:14])([CH3:12])[CH3:13])=[CH:4][CH:3]=1)([O:29][CH2:30][CH3:31])=[O:35])[CH3:34]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 10796Cesium carbonateHCID 283500Diethyl (3-bromopropyl)phosphonateHCID 11831452tert-butyl N-(2-(4-hydroxyphenyl)ethyl)carbamate2×

Produkt 1

HCID 86678287Tert-butyl 4-(3-(diethoxyphosphoryl)propoxy)phenethylcarbamate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a solution of tert-butyl 4-hydroxyphenethylcarbamate (1 eq) in DMF (0.17 M) was added cesium carbonate (5 eq). The resulting mixture was stirred at room temperature for 30 minutes, then diethyl 3-bromopropylphosphonate (1.2 eq) was added into the reaction mixture. The resulting mixture was stirred at room temperature for another 4 hours until tert-butyl 4-hydroxyphenethylcarbamate was consumed. The mixture was then diluted with ethyl acetate, and washed with 5% citric acid three times, saturated NaHCO3 solution, water and brine. The organic layer was then dried over anhydrous Na2SO4, and concentrated en vaccuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 80-100% EtOAc/Hex to give the product as a colorless oil.

Aufarbeitung

  1. customwas consumed
  2. additionThe mixture was then diluted with ethyl acetate
  3. washwashed with 5% citric acid three times, saturated NaHCO3 solution, water and brine
  4. dry with materialThe organic layer was then dried over anhydrous Na2SO4
  5. concentrationconcentrated en vaccuo
  6. customThe crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO)

Quellen und Nachweise

ORD-Eintrag
ord-ae4f523f3675481aaa274089a61af024
Quelldatensatz
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08808703B2

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