4-(Octyloxy)benzoic acid → 4-Octyloxybenzoyl chloride

HRID 21425

Reaktionsgleichung

[CH2:1]([O:9][C:10]1[CH:18]=[CH:17][C:13]([C:14](O)=[O:15])=[CH:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].S(Cl)([Cl:21])=O>>[CH2:1]([O:9][C:10]1[CH:18]=[CH:17][C:13]([C:14]([Cl:21])=[O:15])=[CH:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

Komponenten

Edukt 2

HCID 172314-(Octyloxy)benzoic acid

HCID 24386Thionyl Chloride

Produkt 1

HCID 27602504-Octyloxybenzoyl chloride

Versuchsvorschrift

After 4-n-octyloxybenzoic acid (11 g) and an excessive amount of thionyl chloride were heated under refluxing for 6 hours, unaltered thionyl chloride was distilled off to obtain 4-n-octyloxybenzoic acid chloride.

Aufarbeitung

temperatureunder refluxing for 6 hours
distillationunaltered thionyl chloride was distilled off

Quellen und Nachweise

ORD-Eintrag: ord-5b3123598dd24b67aaa81a9b9a420d75
Quelldatensatz: uspto-grants-1995_06
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US05424005

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