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Toluene → Ethyl 4-(3-bromopropyl)benzoate

HRID 2083111
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2083111
[Br:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=1.S(Cl)(Cl)=O.[C:18]1(C)C=CC=C[CH:19]=1>>[CH2:18]([O:10][C:9](=[O:11])[C:8]1[CH:12]=[CH:13][C:5]([CH2:4][CH2:3][CH2:2][Br:1])=[CH:6][CH:7]=1)[CH3:19]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 1140TolueneHCID 24386Thionyl ChlorideHCID 2377854-(3-Bromopropyl)benzoic acid

Produkt 1

HCID 12748306Ethyl 4-(3-bromopropyl)benzoate

Versuchsvorschrift

100 g 4-(3-Bromo-propyl)-benzoic acid (JACS 65, 2281 (1943) , 400 ml of toluene and 80 ml of thionyl chloride were refluxed for 4 hours. The solvent and the thionyl chloride in excess were removed under reduced pressure and after addition of 400 ml of absolute ethanol to the residue the mixture was heated for one hour to the boiling point. It was evaporated under reduced pressure, the residue was taken up in benzene and washed neutral with a saturated NaHCO3 -solution. The organic phase was distilled off after drying with MgSO4. Boiling point0.1 : 105° - 107° C.

Aufarbeitung

  1. customThe solvent and the thionyl chloride in excess were removed under reduced pressure
  2. additionafter addition of 400 ml of absolute ethanol to the residue the mixture
  3. temperaturewas heated for one hour to the boiling point
  4. customIt was evaporated under reduced pressure
  5. washwashed neutral with a saturated NaHCO3 -solution
  6. distillationThe organic phase was distilled off
  7. dry with materialafter drying with MgSO4
  8. custom105° - 107° C.

Quellen und Nachweise

ORD-Eintrag
ord-bb5681c071f64926bc95c366d4df30ad
Quelldatensatz
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04083990

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