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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70725생성일: 2026년 10월 24일

Hydrochloric Acid → 1-Phenyl-cycloheptene

https://huagongshe.com/ko/reaction/70725

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물CycloheptanoneHCID 10400—
반응물Diphenyl chlorophosphateHCID 75654—
반응물HCID 178425415HCID 178425415—
반응물HCID 178478979HCID 178478979—
촉매HCID 178418476HCID 178418476—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물1-Phenyl-cyclohepteneHCID 27813243%

반응 조건

온도0 °C

반응 단계

Mesitylmagnesium bromide (18.0 mL, 18.0 mmol, 1.0 M in THF) was added over 15 minutes to a solution of cycloheptanone (2.0 g, 17.8 mmol) and diphenyl chlorophosphate (1.1 eq.) in THF (5 mL) at 0° C. The solution was stirred at 0° C. for 30 min, whereafter the solution was allowed to reach room temperature. After stirring the solution for 30 min, dichlorobis(triphenylphosphine)palladium (126 mg, 1 mol %) was added and the solution was warmed to 65° C. Phenylmagnesium chloride (10.8 mL, 1.2 equivalents in THF) was added over 10 minutes, resulting in a gentle reflux of the solvent. After stirring at 65° C. for 30 minutes, the mixture was cooled to rt and poured into a mixture of 3 N HCl (30 mL) and pentane (30 mL). The phases were separated, and the aqueous portion was extracted with pentane (30 mL). The combined organic phase was washed sequentially with 3 N HCl (20 mL), 3 M NaOH (2×20 mL), and brine (20 mL), and dried over MgSO4. Evaporation of the solvent followed by distillation using a Kugelrohr apparatus (oven temperature 100-140° C., 0.065 torr) yielded 1-phenylcycloheptene (1.29 g, 43%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822548B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-cf55e55e22074901a516bc2628059231
출처 메모uspto-grants-2014_09