Acetic Acid → HCID 178491501, Verbindung

HRID 719262

Reaktionsgleichung

Reaktionsgleichung von HRID 719262
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11](=[O:16])[CH2:12][C:13](=[O:15])[CH3:14])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].C(O)(=O)C.[N:21]([O-])=[O:22].[Na+]>O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11](=[O:16])[C:12](=[N:21][OH:22])[C:13](=[O:15])[CH3:14])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]

Komponenten

5

Edukt 3

HCID 176Acetic AcidHCID 3680601-(3,4-Dimethoxyphenyl)butane-1,3-dioneHCID 23668193Sodium Nitrite

Produkt 1

HCID 178491501HCID 178491501, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

5 g of 1-(3,4-dimethoxyphenyl)butane-1,3-dione (41) were initially introduced into 25 ml of acetic acid, and. 1.71 g of sodium nitrite, dissolved in 5 ml of water, were then added dropwise at 15° C. The reaction solution was stirred at RT for 1 h and then remained standing for 2 h. 50 g of ice were added to the solution and the whole was then stored at 0° C. for 12 h, in connection with which the product precipitated out. The product was subsequently filtered off with suction and dried at 50° C. in a drying oven. The following was obtained: 42 C12H13NO5 (251.24); MS (ESI) 252 (M+H)

Aufarbeitung

  1. additionwere then added dropwise at 15° C
  2. waitremained standing for 2 h
  3. waitthe whole was then stored at 0° C. for 12 h, in connection with which
  4. customthe product precipitated out
  5. filtrationThe product was subsequently filtered off with suction
  6. customdried at 50° C. in a drying oven
  7. customThe following was obtained

Quellen und Nachweise

ORD-Eintrag
ord-8165c4347833472ebbe374bd2308dccc
Quelldatensatz
uspto-grants-2006_11
Patentnummer
US07132428B2

Verknüpfte Notizen

Wird geladen…