StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Sodium Hydroxide → HCID 14990622, Verbindung

HRID 2248323
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2248323
[OH-].[Na+].[OH:3][N:4]1[C:8]2[CH:9]=[C:10]([CH:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[OH:14])[CH:11]=[CH:12][C:7]=2[N:6]=[N:5]1>CO>[CH2:12]([O:3][N:4]1[C:8]2[CH:9]=[C:10]([CH:13]([C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=3)[OH:14])[CH:11]=[CH:12][C:7]=2[N:6]=[N:5]1)[CH2:7][CH2:8][CH3:9]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 149906211-hydroxy-alpha-phenyl-1H-benzotriazole-6-methanol

Produkt 1

HCID 14990622HCID 14990622, VerbindungAusbeute 87,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To a stirred solution of 1.2 parts of sodium hydroxide in 40 parts of methanol were added 7.8 parts of 1-hydroxy-α-phenyl-1H-benzotriazole-6-methanol. After concentration, 18 parts of methylbenzene were added to the concentrate. The solvent was evaporated again and the residue was dissolved in 27 parts of N,N-dimethylformamide. 5.52 Parts of 1-iodobutane were added at once and the whole was stirred for 30 minutes at 50° C. After concentration, 30 parts of water were added. The solidified product was filtered off, washed with water and dissolved in dichloromethane. The organic layer was dried, filtered and evaporated. The residue was crystallized from 17.5 parts of 2,2'-oxybispropane. The product was filtered off and dried, yielding 7.8 parts (87.4%) of 1-butoxy-α-phenyl-1H-benzotriazole-6-methanol; mp. 89.2° C. (int. 65).

Aufarbeitung

  1. concentrationAfter concentration, 18 parts of methylbenzene
  2. additionwere added to the concentrate
  3. customThe solvent was evaporated again
  4. dissolutionthe residue was dissolved in 27 parts of N,N-dimethylformamide
  5. addition5.52 Parts of 1-iodobutane were added at once and the whole
  6. concentrationAfter concentration, 30 parts of water
  7. additionwere added
  8. filtrationThe solidified product was filtered off
  9. washwashed with water
  10. dissolutiondissolved in dichloromethane
  11. customThe organic layer was dried
  12. filtrationfiltered
  13. customevaporated
  14. customThe residue was crystallized from 17.5 parts of 2,2'-oxybispropane
  15. filtrationThe product was filtered off
  16. customdried

Quellen und Nachweise

ORD-Eintrag
ord-bb4ac646f36647838de69083f9b0d1f5
Quelldatensatz
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05039677

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion