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

Lithium Chloride → Methyl 3-(2-bromophenyl)propanoate

HRID 234075
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 234075
[Br:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[CH2:4][CH:5](C(OC)=O)[C:6]([O:8][CH3:9])=[O:7].[Cl-].[Li+]>CS(C)=O.O>[Br:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[CH2:4][CH2:5][C:6]([O:8][CH3:9])=[O:7]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 433294Lithium ChlorideHCID 23358293Dimethyl [(2-bromophenyl)methyl]propanedioate

Produkt 1

HCID 15712815Methyl 3-(2-bromophenyl)propanoateAusbeute 68,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 679Dimethyl SulfoxideLösungsmittelHCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
160 °C

Versuchsvorschrift

Dimethyl 2-(2-bromobenzyl)malonate (54.25 g) was dissolved in a mixture of dimethylsulfoxide (220 ml) and water (3.24 ml), and lithium chloride (15.27 g) was added. The mixture was stirred at 160° C. of a bath temperature for 7.5 hours. After the reaction mixture was left standing for cooling, the solvent was removed by distillation under reduced pressure. The residual concentrate was poured into water, extracted with toluene. The organic layer obtained was washed twice with water and once with a saturated aqueous saline, dried over sodium sulfate, the solvent was removed by distillation under reduced pressure, and the residual concentrate was distilled under reduced pressure (96°-98° C./0.5 mmHg) to give the title compound (30.05 g).

Aufarbeitung

  1. additionwas added
  2. waitAfter the reaction mixture was left
  3. temperaturefor cooling
  4. customthe solvent was removed by distillation under reduced pressure
  5. concentrationThe residual concentrate
  6. additionwas poured into water
  7. extractionextracted with toluene
  8. customThe organic layer obtained
  9. washwas washed twice with water and once with a saturated aqueous saline
  10. dry with materialdried over sodium sulfate
  11. customthe solvent was removed by distillation under reduced pressure
  12. concentrationthe residual concentrate
  13. distillationwas distilled under reduced pressure (96°-98° C./0.5 mmHg)

Quellen und Nachweise

ORD-Eintrag
ord-1a8a120b80ac42d28f83f1bfff1d0b12
Quelldatensatz
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05594081

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion