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Cornforth reagent → tert-Butyl methyl(4-oxobutyl)carbamate

HRID 1165035
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1165035
[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[OH:22][CH2:23][CH2:24][CH2:25][CH2:26][N:27]([CH3:35])[C:28](=[O:34])[O:29][C:30]([CH3:33])([CH3:32])[CH3:31]>ClCCl>[CH3:35][N:27]([CH2:26][CH2:25][CH2:24][CH:23]=[O:22])[C:28](=[O:34])[O:29][C:30]([CH3:33])([CH3:31])[CH3:32]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 2724130Cornforth reagentHCID 14854943tert-Butyl (4-hydroxybutyl)(methyl)carbamate

Produkt 1

HCID 15078448tert-Butyl methyl(4-oxobutyl)carbamateAusbeute 6,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a stirred and cooled (<10° C.) solution of 150 parts of pyridinium dichromate in 1300 parts of dichloromethane was added dropwise a solution of 50 parts of (1,1-dimethylethyl) (4-hydroxybutyl)methylcarbamate in 91 parts of dichloromethane. Upon complete addition, stirring was continued for 3 hours in the presence of 112 parts of molecular sieves of 4A at room temperature. The reaction mixture was filtered over magnesium sulfate, washed with 1,1'-oxybisethane and the filtrate was evaporated. The residue was purified by column chromatography over silica gel using dichloromethane as eluent. The pure fractions were collected and the eluent was evaporated. The residue was taken up in methylbenzene and the whole was evaporated again, yielding 3.5 parts (6.9%) of (1,1-dimethylethyl) methyl(4-oxobutyl)carbamate as a residue (interm. 7).

Aufarbeitung

  1. additionUpon complete addition
  2. stirringstirring
  3. filtrationThe reaction mixture was filtered over magnesium sulfate
  4. washwashed with 1,1'-oxybisethane
  5. customthe filtrate was evaporated
  6. customThe residue was purified by column chromatography over silica gel
  7. customThe pure fractions were collected
  8. customthe eluent was evaporated
  9. customthe whole was evaporated again

Quellen und Nachweise

ORD-Eintrag
ord-0014caa4e6104baab04266c7a31755d2
Quelldatensatz
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04906643

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