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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2396398생성일: 2026년 10월 27일

Acetyl chloride → Benzoic anhydride

https://huagongshe.com/reaction/2396398

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물Benzoyl chlorideHCID 7412—
반응물Acetic AnhydrideHCID 7918—
반응물Pivaloyl chlorideHCID 62493—
반응물Acrylic anhydrideHCID 74919—
반응물Pivaloylpivaloyl chlorideHCID 54295827—
생성물Benzoic anhydrideHCID 7167—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05491244
출처 데이터셋uspto-grants-1996_02
ORD IDord-cc463f6abaad48b9a0e88db179428b24
출처 메모uspto-grants-1996_02