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HRID 1111286作成日:2026年10月26日

Potassium Iodide → HCID 22151947、化合物

https://huagongshe.com/reaction/1111286

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Dichloroacetic AcidHCID 6597—
反応物2,2'-Dihydroxy-4-methoxybenzophenoneHCID 8569—
反応物Potassium CarbonateHCID 11430—
溶媒WaterHCID 962—
溶媒IsopropanolHCID 3776—
生成物HCID 22151947HCID 22151947—

反応手順

(2-Hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)methanone (16.1 g, 65.9 mmol), 36.5 g (258 mmol) of potassium carbonate, and 3.00 g (18 mmol) of potassium iodide were suspended in 250 ml of 2-propanol and heated with stirring. Dichloroacetic acid (6.00 ml, 72.6 mmol) was added slowly with a syringe and the mixture heated at reflux with stirring. After 48 hours another 5.00 ml of dichloroacetic acid was added and the reaction continued for another 48 hours. The mixture was then allowed to cool and was concentrated by evaporation under reduced pressure to obtain a solid residue. The residue was dissolved in 500 ml of water and the solution extracted with 200 ml of ether. The aqueous layer was then acidified with concentrated aqueous hydrochloric acid and then extracted twice with 500 ml portions of ether and once with 300 ml of ethyl acetate. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain 3-methoxy- 12H-dibenzo[d,g][1,3]dioxocin-12-one-6-carboxylic acid as a semi-solid residue. The proton nmr spectrum was consistent with the assigned structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04979978
出典データセットuspto-grants-1990_12
ORD IDord-8270aedd607e45e7bb9c163eec5d0b1a
出典メモuspto-grants-1990_12