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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132716생성일: 2026년 10월 26일

Pyridine → 1,4-Bis(benzoyloxymethyl)cyclohexane

https://huagongshe.com/reaction/132716

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Benzoyl chlorideHCID 7412—
반응물1,4-CyclohexanedimethanolHCID 7735—
반응물TetrahydrofuranHCID 8028—
생성물1,4-Bis(benzoyloxymethyl)cyclohexaneHCID 11824495%

반응 단계

To 0.03 mol 1,4-dihydroxymethylcyclohexane were added 30 ml tetrahydrofuran and 0.09 mol pyridine, then added 0.075 mol benzoyl chloride with stirring. The reaction was heated refluxing for 4 hours, cooled and added 20 ml saturated saline. The reaction mixture was extracted with ethyl acetate, and the extract was dried over anhydrous sodium sulfate, filtered. After removing solvent, the crude was purified by recrystallization from ethyl acetate and petroleum ether (2:1 v/v) to give 1,4-di(benzoyloxymethyl)cyclohexane as a white solid. The yield was 95%, and m.p. was 111-113° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388061B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-b5d3024eff4646769e9da25fb1b1ae6a
출처 메모uspto-grants-2008_06