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Methanol → Methyl 2-(4-Bromophenoxymethyl)benzoic Acid

HRID 1515223
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1515223
[OH-].[Na+].[Br:3][C:4]1[CH:21]=[CH:20][C:7]([O:8][CH2:9][C:10]2[CH:19]=[CH:18][CH:17]=[CH:16][C:11]=2[C:12]([O:14]C)=[O:13])=[CH:6][CH:5]=1.[CH3:22]O>>[CH3:22][C:19]1[C:10]([CH2:9][O:8][C:7]2[CH:20]=[CH:21][C:4]([Br:3])=[CH:5][CH:6]=2)=[C:11]([CH:16]=[CH:17][CH:18]=1)[C:12]([OH:14])=[O:13]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 53995976Methyl 2-((4-bromophenoxy)methyl)benzoate

Produkt 1

HCID 68526746Methyl 2-(4-Bromophenoxymethyl)benzoic AcidAusbeute 84 %

Versuchsvorschrift

A 2 mol/L aqueous sodium hydroxide solution (250 mL) was added to a methanol (1 L) solution of methyl 2-(4-bromophenoxymethyl)-benzoate (139 g, 432 mmol), and the mixture was stirred overnight while heating under reflux. Methanol was distilled off under a reduced pressure, and a 6 mol/L hydrochloric acid was added to the residue obtained to precipitate the crystals, and the precipitated crystals were collected by filtration, and sufficiently washed with water. The crystals were dried over phosphorus pentoxide at 50° C., to give 112 g (84%) of the captioned compound.

Aufarbeitung

  1. temperaturewhile heating
  2. temperatureunder reflux
  3. distillationMethanol was distilled off under a reduced pressure
  4. additiona 6 mol/L hydrochloric acid was added to the residue
  5. customobtained
  6. customto precipitate the crystals
  7. filtrationthe precipitated crystals were collected by filtration
  8. washsufficiently washed with water
  9. dry with materialThe crystals were dried over phosphorus pentoxide at 50° C.

Quellen und Nachweise

ORD-Eintrag
ord-d032d885cf694bdf85fbc0952f03b1c6
Quelldatensatz
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08222419B2

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