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Hydrochloric Acid → 1-[(3-Acetyl-4-hydroxyphenyl)methyl]-2-pyrrolidinone

HRID 1591202
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1591202
[H-].[Na+].[NH:3]1[CH2:7][CH2:6][CH2:5][C:4]1=[O:8].Cl[CH2:10][C:11]1[CH:12]=[CH:13][C:14]([OH:20])=[C:15]([C:17](=[O:19])[CH3:18])[CH:16]=1.Cl>CN(C)C=O>[C:17]([C:15]1[CH:16]=[C:11]([CH2:10][N:3]2[CH2:7][CH2:6][CH2:5][C:4]2=[O:8])[CH:12]=[CH:13][C:14]=1[OH:20])(=[O:19])[CH3:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 120252-PyrrolidoneHCID 24758Sodium hydrideHCID 225570132-Acetyl-4-chloromethyl phenol

Produkt 1

HCID 190454421-[(3-Acetyl-4-hydroxyphenyl)methyl]-2-pyrrolidinoneAusbeute 82,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel
3×

Versuchsvorschrift

To a suspension of sodium hydride (60% dispersion in mineral oil, 0.80 g, 20.0 mmol) in 15 mL dry dimethylformamide under argon, cooled in an ice-bath was added dropwise a solution of 2-pyrrolidinone (1.70 g, 20.0 mmol) in 5 mL dimethylformamide. The ice-bath was removed, the mixture was stirred 30 minutes, and a solution of 5'-(chloromethyl)-2'-hydroxyacetophenone (1.85 g, 10.0 mmol) in 5 mL dimethylformamide was added dropwise. The mixture was stirred four hours, poured into 75 mL ice water, acidified with 7 mL 3N hydrochloric acid, and extracted with methylene chloride (3×75 mL). The extract was washed with water (25 mL) and brine, dried over Na2SO4, and filtered. The filtrate was concentrated in vacuo to give crude product which was purified by flash chromatography on silica gel eluting with 2:98 methanol:chloroform to give 1.92 g (82%) product as a viscous oil.

Aufarbeitung

  1. temperaturecooled in an ice-bath
  2. customThe ice-bath was removed
  3. stirringThe mixture was stirred four hours
  4. extractionextracted with methylene chloride (3×75 mL)
  5. washThe extract was washed with water (25 mL) and brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated in vacuo
  9. customto give crude product which
  10. customwas purified by flash chromatography on silica gel eluting with 2:98 methanol

Quellen und Nachweise

ORD-Eintrag
ord-7154daecb95d4eebb7534b147ea5390c
Quelldatensatz
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05206240

Notizen zur Reaktion

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