Sodium Hydroxide → 4-(3-Methylphenyl)benzoic acid

HRID 1070418

Reaktionsgleichung

Reaktionsgleichung von HRID 1070418
C([O:3][C:4]([C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([CH3:18])[CH:13]=2)=[CH:8][CH:7]=1)=[O:5])C.[OH-].[Na+]>O1CCCC1>[CH3:18][C:14]1[CH:13]=[C:12]([C:9]2[CH:10]=[CH:11][C:6]([C:4]([OH:5])=[O:3])=[CH:7][CH:8]=2)[CH:17]=[CH:16][CH:15]=1

Komponenten

4

Versuchsvorschrift

A solution of 3′-methyl-[1,1′-biphenyl]-4-carboxylic acid ethyl ester of Step A (3.3 g, 13.7 mmol) in tetrahydrofuran (40 mL) and 1 N sodium hydroxide (27.5 mL, 27.5 mmol) was heated at reflux overnight. After cooling, the reaction was concentrated in vacuo. The residue was acidified with 2N hydrochloric acid to yield a white solid which was collected by filtration and dried under vacuum to provide the title compound (2.9 g, 99.7%) as a white solid, m.p. 198-200° C.

Aufarbeitung

  1. temperatureat reflux overnight
  2. temperatureAfter cooling
  3. concentrationthe reaction was concentrated in vacuo
  4. customto yield a white solid which
  5. filtrationwas collected by filtration
  6. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-b790c093620e4ecda36bbd4d136eddea
Quelldatensatz
uspto-grants-2005_06
Patentnummer
US06903091B2

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