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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223803생성일: 2026년 10월 26일

Iodoacetic Acid → [(5,6-Dichloro-9a-ethyl-3-oxo-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]acetic acid

https://huagongshe.com/reaction/223803

반응식

참여 물질

역할이름HCID투입량
반응물Iodoacetic AcidHCID 5240—
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물5,6-dichloro-9a-ethyl-7-hydroxy-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 12806935—
용매WaterHCID 962—
생성물[(5,6-Dichloro-9a-ethyl-3-oxo-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]acetic acidHCID 12806939—

반응 조건

온도50 °C

반응 단계

5,6-Dichloro-9a-ethyl-7-hydroxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one, (Example 1, Step C) (15 gm., 0.048 mole), potassium carbonate (13.3 gm., 0.096 mole), dimethylformamide (100 ml.) and iodoacetic acid (10.6 gm., 0.057 mole) is stirred at room temperature for 24 hours. The reaction mixture is poured into water (150 ml.), stirred, warmed to 50° C., filtered and the filtrate acidified with 6 N hydrochloric acid to obtain [(5,6-dichloro-9a-ethyl-3-oxo-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]acetic acid, which after recrystallization from acetic acid, melts at 237° C.-238° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04356313
출처 데이터셋uspto-grants-1982_10
ORD IDord-68a1c8086cfb4b6e8c568bb8f6c83c13
출처 메모uspto-grants-1982_10