Sulfuric Acid → Benzoic acid, 2-chloro-4-hydroxy-, 4-pentylphenyl ester

HRID 918551Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 918551
[CH2:1]([C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH2:4][CH3:5].[Cl:13][C:14]1[CH:22]=[C:21]([OH:23])[CH:20]=[CH:19][C:15]=1[C:16](O)=[O:17].S(=O)(=O)(O)O.B(O)(O)O>C1(C)C=CC=CC=1>[Cl:13][C:14]1[CH:22]=[C:21]([OH:23])[CH:20]=[CH:19][C:15]=1[C:16]([O:12][C:9]1[CH:8]=[CH:7][C:6]([CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])=[CH:11][CH:10]=1)=[O:17]

Komponenten

6

Versuchsvorschrift

To a suspension of p-pentylphenol (0.15 mole) and 2-chloro-4-hydroxybenzoic acid (0.10 mole) in toluene (500 ml.) is added concentrated sulfuric acid (0.5 g.) and boric acid (0.31 g.) (5 mole percent). The reaction mixture is refluxed for 29 hours under a Dean-Stark trap. The solvent is then removed under reduced pressure and the product is washed with ligroin. The resulting 4-pentylphenyl 2-chloro-4-hydroxybenzoate is recrystallized from an ethanol/water mixture to give 25.6 g., 81% of pure product, m.p. 149°-151°C.

Aufarbeitung

  1. temperatureThe reaction mixture is refluxed for 29 hours under a Dean-Stark trap
  2. customThe solvent is then removed under reduced pressure
  3. washthe product is washed with ligroin
  4. customThe resulting 4-pentylphenyl 2-chloro-4-hydroxybenzoate is recrystallized from an ethanol/water mixture
  5. customto give 25.6 g

Quellen und Nachweise

ORD-Eintrag
ord-57f01a4ad51941caaf854eb1358aa1de
Quelldatensatz
uspto-grants-1976_07
Patentnummer
US03971824

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