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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397162생성일: 2026년 10월 24일

1,4-Dioxaspiro[4.5]decan-8-one → 8-[(4-Fluorophenyl)methylene]-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/ko/reaction/397162

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참여 물질

역할이름HCID투입량
반응물1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
반응물(4-Fluorobenzyl)triphenylphosphonium chlorideHCID 2733554—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물8-[(4-Fluorophenyl)methylene]-1,4-dioxaspiro[4.5]decaneHCID 1213395079.3%

반응 조건

온도0 °C

반응 단계

To a stirring solution of 4-fluorophenylmethyl triphenylphosphonium chloride (39 g, 96 mmol, Lancaster) in 500 mL of dry THF at −78° C. was added 1 M potassium t-butoxide in THF (106 mL, 106 mmol, Aldrich). The reaction was stirred for 30 min and then warmed to 0° C. The reaction was stirred for 30 min and then 1,4-cyclohexanedione mono-ethylene ketal (15.0 g, 96 mmol, Aldrich) was added. After 30 min, the reaction was warmed to room temperature and allowed to stir overnight. The reaction was heated to reflux for 4 h and then cooled to room temperature. The reaction was quenched with saturated ammonium chloride (500 mL) and ethyl acetate (500 mL). The organic layer was separated, washed with brine, dried over sodium sulfate, and conc in vacuo to a white solid. The solid was purified by flash chromatography (SiO2, 19:1 hexanes:ethyl acetate) to yield 18.9 g of a colorless oil. MS (ESI) 251 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608227B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-157c8a3c8a5045bd96f3c3605b092e44
출처 메모uspto-grants-2003_08