돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132728생성일: 2026년 10월 26일

Pyridine → HCID 23126022, 화합물

https://huagongshe.com/reaction/132728

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Benzoyl chlorideHCID 7412—
반응물Propionyl chlorideHCID 62324—
반응물9H-Fluorene-9,9-dimethanolHCID 345022—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물HCID 23126022HCID 2312602279%

반응 단계

To 4.5 g (0.02 mol) 9,9-di(hydroxymethyl)fluorene were added 30 ml tetrahydrofuran, and added 3.3 ml (0.03 mol) pyridine with stirring. To the resulting homogenous mixture was added slowly 2.3 ml (0.02 mol) benzoyl chloride, and the mixture was stirred at temperature for 1 hour, then heated refluxing for 5 hours. Next, the mixture was cooled to room temperature, and 20 ml tetrahydrofuran and 3.3 ml(0.03 mol) pyridine were added with stirring. To the resulting homogenous mixture was slowly added 1.8 ml (0.02 mol) propionyl chloride, and the mixture was stirred at room temperature for 1 hour, and heated refluxing for 5 hours. Then 30 ml water was added to dissolve the resulting salt. The mixture was extracted with toluene. The organic phase was separated, washed with saturated saline for two times, and dried over anhydrous sodium sulfate. The solvent was removed. Recrystallization from ethyl acetate gave 9-(benzoyloxymethyl)-9-(propionyloxymethyl)fluorene as a white crystal, and the yield was 79%. 1HNMR: δ (ppm) 1.23(t, 3H, CH3), 2.39(m, 2H, CH2), 4.48(s, 2H, COOCH2), 4.62(s, 2H, OCH2 linking with benzoyl), 7.33-8.03(m, 13H, ArH)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388061B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-9ecee5bddf50403e821309d6521d6031
출처 메모uspto-grants-2008_06