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Hydrochloric Acid → 3'-Acetylaminomethylacetophenone

HRID 1734016
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1734016
C([C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][CH:13]=1)[CH2:6][NH:7][C:8](=[O:10])[CH3:9])#N.C[Mg]Br.O.Cl.CC[O:21][CH2:22][CH3:23]>C(Cl)Cl.O1CCCC1>[C:8]([NH:7][CH2:6][C:5]1[CH:4]=[C:3]([C:22](=[O:21])[CH3:23])[CH:13]=[CH:12][CH:11]=1)(=[O:10])[CH3:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 313Hydrochloric AcidHCID 962WaterHCID 3283Diethyl EtherHCID 19439673HCID 19439673, VerbindungHCID 178418573HCID 178418573, Verbindung

Produkt 1

HCID 107977903'-Acetylaminomethylacetophenone

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344
Dichloromethane
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of N-(3-cyanobenzyl)acetamide (7.7 g) in methylene dichloride (150 ml) and tetrahydrofuran (50 ml) was added dropwise a solution of methyl magnesium bromide in ether (3 mol/l, 52 ml) at 10° to 20° C. under stirring and the resulting mixture was stirred at the same condition for 6 hours. The reaction mixture was poured into water and the resultant mixture was adjusted to pH 7 with 6N hydrochloric acid and extracted with ethyl acetate. The extract was washed with brine and magnesium sulfate. The solvent was evaporated in vacuo and the residue was subjected to column chromatography on silica gel. The fractions eluted with a mixture of chloroform and ethyl acetate (8:2) were collected and the solvent was evaporated in vacuo to give 3'-(acetylaminomethyl)acetophenone (4.7 g) (oil).

Aufarbeitung

  1. stirringthe resulting mixture was stirred at the same condition for 6 hours
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with brine and magnesium sulfate
  4. customThe solvent was evaporated in vacuo
  5. washThe fractions eluted with a mixture of chloroform and ethyl acetate (8:2)
  6. customwere collected
  7. customthe solvent was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-6e0d0d76fc7e4cbb8631122fa976af01
Quelldatensatz
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05532258

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