2,5-Dichloro-3-nitrobenzoic acid → 2,5-Dichloro-3-nitrobenzoyl chloride

HRID 1532451Notizen

Reaktionsgleichung

[Cl:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:8]([Cl:14])=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:17])=O>>[Cl:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:8]([Cl:14])=[CH:7][C:3]=1[C:4]([Cl:17])=[O:5]

Komponenten

Edukt 2

HCID 69512,5-Dichloro-3-nitrobenzoic acid

HCID 24386Thionyl Chloride

Produkt 1

HCID 101063862,5-Dichloro-3-nitrobenzoyl chlorideAusbeute 87,5 %

Versuchsvorschrift

A mixture of 5.0 parts of 2,5-dichloro-3-nitrobenzoic acid and 16.2 parts of thionyl chloride was refluxed for 24 hours under argon. The reaction mixture was evaporated, yielding 4.74 parts (87.5%) of 2,5-dichloro-3-nitrobenzoyl chloride (interm. 66).

Aufarbeitung

temperaturewas refluxed for 24 hours under argon
customThe reaction mixture was evaporated

Quellen und Nachweise

ORD-Eintrag: ord-7b546e05a10c48ec8a242c2f379bb601
Quelldatensatz: uspto-grants-2001_03
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US06201119B1

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