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

p-Toluenesulfonic acid → HCID 53789449, Verbindung

HRID 1440642
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1440642
[C:1]([O:7][CH3:8])(=[O:6])[CH:2]([CH2:4][OH:5])[OH:3].[Br:9][CH:10](O)C.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[C:1]([O:7][CH2:8][CH2:10][Br:9])(=[O:6])[CH:2]([CH2:4][OH:5])[OH:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 6101p-Toluenesulfonic acidHCID 140003Methyl 2,3-dihydroxypropanoateHCID 14202443Ethanol, 1-bromo-

Produkt 1

HCID 53789449HCID 53789449, VerbindungAusbeute 92 %

Versuchsvorschrift

A mixture of methyl glycerate (2 g, 0.17 moles) and bromoethanol (5.28 g, 0.42 moles was heated at 60° C. under nitrogen in the presence of a catalytic amount of p-toluene sulfonic acid for 10 h. The excess bromoethanol was removed on rotary evaporator under reduced pressure. The crude mixture was diluted with large volume of chloroform (100 mL) and the free acid was neutralized by adding anhydrous sodium carbonate. Filtration and removal of the solvent gave the crude product which was purified by chromatography on a silica gel column eluting with chloroform:methanol (9:1). Removal of the solvent on a rotary evaporator gave bromoethyl glycerate (3.26 g, 92% yield) which showed the following characteristics: 1H NMR (200 MHz, CDCl3), δ 3.52 (m, 2H, CH2Br), 3.90 (m, 2H,CO2CH2), 4.27 (s, 2H, OH), 4.36 (m, 2H, CH2OH), 4.52 (m, 1 H, CH), 13C NMR (50 MHz, CDCl3) δ 28.42, 63.76, 64.50, 71.58, 172.13.

Aufarbeitung

  1. customThe excess bromoethanol was removed on rotary evaporator under reduced pressure
  2. additionThe crude mixture was diluted with large volume of chloroform (100 mL)
  3. additionby adding anhydrous sodium carbonate
  4. filtrationFiltration and removal of the solvent
  5. customgave the crude product which
  6. customwas purified by chromatography on a silica gel column
  7. washeluting with chloroform:methanol (9:1)
  8. customRemoval of the solvent
  9. customon a rotary evaporator

Quellen und Nachweise

ORD-Eintrag
ord-927c7dd6a9c54b4aab3a94c48f4a6aa6
Quelldatensatz
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05500139

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion