Hydrochloric Acid → Nonanoic acid 4-hydroxyphenyl ester

HRID 1165724

Reaktionsgleichung

Reaktionsgleichung von HRID 1165724
[C:1](Cl)(=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].[C:12]1([CH:19]=[CH:18][C:16]([OH:17])=[CH:15][CH:14]=1)[OH:13].Cl>N1C=CC=CC=1>[CH2:2]([C:1]([O:13][C:12]1[CH:19]=[CH:18][C:16]([OH:17])=[CH:15][CH:14]=1)=[O:10])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9]

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 785HydroquinoneHCID 69819Nonanoyl chloride

Produkt 1

HCID 573704Nonanoic acid 4-hydroxyphenyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Versuchsvorschrift

After adding 17 g of nonanic acid chloride to 200 ml of pyridine dissolved with 47 g of hydroquinone, the mixture was heated for 2 hours. Following neutralization of hydrogen chloride, the crude of 4-octylcarbonyloxyphenol was obtained by extracting with chloroform. The crude compound was purified by passing through silica-gel column to obtain pure 4-octylcarbonyloxyphenol (J). (I) was reacted with (J) to obtain the compound (G) same procedure as example 14. (G) was a smectic liquid crystal compound having the SC* phase. The phase transition points of (G) were shown in table 4.

Aufarbeitung

  1. temperaturethe mixture was heated for 2 hours

Quellen und Nachweise

ORD-Eintrag
ord-e0afdb7c0b6a400f944dfb2c06e48da0
Quelldatensatz
uspto-grants-1990_03
Patentnummer
US04911861

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