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Water → 2-(2-Bromo-3-methylphenyl)acetic acid

HRID 1006698
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1006698
[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[CH2:4][C:5]#N.S(=O)(=O)(O)[OH:13].[OH2:17]>C(OCC)C>[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[CH2:4][C:5]([OH:13])=[O:17]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962Water2×HCID 1118Sulfuric AcidHCID 226726132-(2-Bromo-3-methylphenyl)acetonitrile

Produkt 1

HCID 183574462-(2-Bromo-3-methylphenyl)acetic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

2-bromo-3-methylbenzylcyanid (8.8 g, 42 mmol) was added to a mixture of conc sulfuric acid (50 ml) and water (60 ml) and was refluxed overnight. Water (150 ml) and diethyl ether were added and the organic layer was separated. To the organic layer was added a saturated sodium bicarbonate solution and the aqueous layer was separated. The aqueous layer was made acidic by additon of conc sulfuric acid. The acidic water solution was extracted with diethyl ether and the organic layer was washed with water, dried (Na2SO4) and evaporated under reduced pressure to give 6.5 g of the title compound.

Aufarbeitung

  1. temperaturewas refluxed overnight
  2. customthe organic layer was separated
  3. additionTo the organic layer was added a saturated sodium bicarbonate solution
  4. customthe aqueous layer was separated
  5. extractionThe acidic water solution was extracted with diethyl ether
  6. washthe organic layer was washed with water
  7. dry with materialdried (Na2SO4)
  8. customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-a531a3da22ea44cdbed049cffe203659
Quelldatensatz
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06790960B2

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