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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1824666생성일: 2026년 10월 27일

Epichlorohydrin → 2-[(4-Benzoylphenoxy)methyl]oxirane

https://huagongshe.com/reaction/1824666

반응식

참여 물질

역할이름HCID투입량
반응물EpichlorohydrinHCID 7835—
반응물Potassium CarbonateHCID 11430—
반응물4-HydroxybenzophenoneHCID 14347—
용매AcetoneHCID 180—
생성물2-[(4-Benzoylphenoxy)methyl]oxiraneHCID 352816—

반응 단계

As illustrated in FIG. 6, 100 mL of dried acetone were added to a dry, 250-mL round bottom flask, equipped with a magnetic stirrer, along with 15.05 grams of 4-hydroxybenzophenone, 32.1 grams of epichlorohydrin, and 6.2 grams of potassium carbonate. The solution was heated to reflux for 6 hours and then cooled to room temperature. The precipitated potassium chloride was filtered off, and the solution was evaporated to remove excess epichlorohydrin. The crude product was recrystallized from methanol. 1H NMR data confirmed the formation of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07045366B2
출처 데이터셋uspto-grants-2006_05
ORD IDord-11abb5634ed142ee9bd12b16b8fc0da6
출처 메모uspto-grants-2006_05