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Sulfuric Acid → p-n-Octadecyloxybenzoic acid

HRID 21434
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 21434
[CH2:1]([O:19][C:20]1[CH:29]=[CH:28][C:23]([C:24]([O:26]C)=[O:25])=[CH:22][CH:21]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].S(=O)(=O)(O)O>C(O)(=O)C>[CH2:1]([O:19][C:20]1[CH:21]=[CH:22][C:23]([C:24]([OH:26])=[O:25])=[CH:28][CH:29]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 1118Sulfuric AcidHCID 4189536Methyl 4-(octadecyloxy)benzoate

Produkt 1

HCID 139993p-n-Octadecyloxybenzoic acidAusbeute 82,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

A mixture containing methyl 4-octadecyloxybenzoate (30 g) and acetic acid (10 ml) was warmed until a solution was obtained. To this solution was added concentrated sulfuric acid (3 ml), and the mixture heated to slowly distill off the methyl acetate. This distillation was carried out over a period of 40 minutes. The solution was then cooled just below the boiling point and stirred for an additional 30 minutes. The hot reaction mixture was poured onto cold water and the solid filtered and dried. The product was then slurried in methylene chloride (100 ml) then filtered. The solid was recrystallized from 2-butanone to give 4-octadecyloxybenzoic acid (24 g).

Aufarbeitung

  1. temperaturewas warmed until a solution
  2. customwas obtained
  3. temperaturethe mixture heated
  4. distillationto slowly distill off the methyl acetate
  5. distillationThis distillation
  6. temperatureThe solution was then cooled just below the boiling point
  7. additionThe hot reaction mixture was poured onto cold water
  8. filtrationthe solid filtered
  9. customdried
  10. filtrationthen filtered
  11. customThe solid was recrystallized from 2-butanone

Quellen und Nachweise

ORD-Eintrag
ord-2a7c3976ac664099ac53a5193537f233
Quelldatensatz
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05424183

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