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HRID 223821作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/223821

反応式

関与物質

役割名称HCID仕込み量
反応物Iodoacetic AcidHCID 5240—
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物5,6-dichloro-9a-ethyl-7-hydroxy-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 12806935—
溶媒WaterHCID 962—
生成物[(5,6-Dichloro-9a-ethyl-3-oxo-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]acetic acidHCID 12806939—

反応条件

温度50 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04356314
出典データセットuspto-grants-1982_10
ORD IDord-5b60d7e8a4bb44abadef6893b493c914
出典メモuspto-grants-1982_10