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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2396398Erstellt: 26. Oktober 2026

Acetyl chloride → Benzoic anhydride

https://huagongshe.com/reaction/2396398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetyl chlorideHCID 6367—
EduktBenzoyl chlorideHCID 7412—
EduktAcetic AnhydrideHCID 7918—
EduktPivaloyl chlorideHCID 62493—
EduktAcrylic anhydrideHCID 74919—
EduktHCID 54295827HCID 54295827—
ProduktBenzoic anhydrideHCID 7167—

Reaktionsschritte

As seen below, benzoyl chloride, acetyl chloride and pivaloyl chloride were tested for use in the present invention. The best results were obtained with benzoyl chloride, which provided a yield of the acrylic anhydride of 77.2%. Acetyl chloride gave a less preferred product mixture that comprised 50% mixed anhydride, 25% acetic anhydride and 25% acrylic anhydride; the pivaloyl chloride reaction also gave a less preferred product mixture that comprised 50% mixed anhydride, 30% pivaloyl anhydride and 20% acrylic anhydride, based on gas chromatographic analysis. Benzoyl chloride is also more preferred than acetyl chloride and trimethyacetyl (pivaloyl) chloride, because the benzoyl chloride reaction yields benzoic anhydride which has a much greater boiling point than acrylic anhydride, facilitating the separation of the acrylic anhydride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05491244
Quelldatensatzuspto-grants-1996_02
ORD IDord-cc463f6abaad48b9a0e88db179428b24
Quellennotizuspto-grants-1996_02