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Sodium Hydroxide → O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-beta-hydroxytyrosine

HRID 1587284
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1587284
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:18]=[CH:17][C:8]([CH:9]([OH:16])[C@@H:10]([C:13]([OH:15])=[O:14])[NH:11][CH3:12])=[CH:7][CH:6]=1.C[Si](C([Si](C)(C)C)C(N)=O)(C)C.[N+:31]([C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=1[S:40]Cl)([O-:33])=[O:32].[OH-].[Na+]>ClCCl>[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:6]=[CH:7][C:8]([CH:9]([OH:16])[C@@H:10]([C:13]([OH:15])=[O:14])[N:11]([CH3:12])[S:40][C:35]2[CH:36]=[CH:37][CH:38]=[CH:39][C:34]=2[N+:31]([O-:33])=[O:32])=[CH:17][CH:18]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 14798Sodium HydroxideHCID 243192-Nitrobenzenesulfenyl chloride2×HCID 11708267Bistrimethylsilylacetamid2×HCID 53901170O-methoxymethyl-N-methyl-beta-hydroxytyrosine

Produkt 1

HCID 54196694O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-beta-hydroxytyrosineAusbeute 85 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of O-methoxymethyl-N-methyl-β-hydroxytyrosine (15.1 g) and bis(trimethylsilyl)acetamide (25 ml) in dichloromethane (150 ml) was added a solution of 2-nitrophenylsulfenyl chloride (11.2 g) in dichloromethane (50 ml). After stirring for 2 hours at 0° C., bis(trimethylsilyl)acetamide (10 ml) and 2-nitrophenylsulfenyl chloride (5.6 g) was added to the solution. The mixture was stirred for 3 hours at room temperature and added to 1N-sodium hydroxide (200 ml). The organic layer was washed with water (300 ml) and the aqueous solutions were combined. After the aqueous solution was acidified with diluted hydrochloric acid, the product was extracted with ethyl acetate (300 ml) and the extract was washed with water (100 ml×3). After the solution was dried over magnesium sulfate, the solvent was removed in vacuo to give O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-β-hydroxytyrosine (20.5 g).

Aufarbeitung

  1. stirringThe mixture was stirred for 3 hours at room temperature
  2. washThe organic layer was washed with water (300 ml)
  3. extractionthe product was extracted with ethyl acetate (300 ml)
  4. washthe extract was washed with water (100 ml×3)
  5. dry with materialAfter the solution was dried over magnesium sulfate
  6. customthe solvent was removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-51a3820cfad94e8ba290507c4c7ed349
Quelldatensatz
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05217952

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