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HRID 340875作成日:2026年10月25日

Potassium Iodide → (E)-Hex-3-ene-2,5-diol isophthaloyl chloride 5-acetoxy isophthaloyl chloride

https://huagongshe.com/reaction/340875

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Isophthaloyl chlorideHCID 7451—
反応物DabcoHCID 9237—
反応物ButanediolHCID 165788—
反応物3-Hexene-2,5-diolHCID 5363299—
反応物1,3-Benzenedicarbonyl dichloride, 5-(acetyloxy)-HCID 10515530—
溶媒PyridineHCID 1049—
生成物(E)-Hex-3-ene-2,5-diol isophthaloyl chloride 5-acetoxy isophthaloyl chlorideHCID 131732093—

反応手順

A solution of (E)-hex-3-ene-2,5-diol (122) (0.441 g, 3.8 mmol), isophthaloyl chloride (115) (0.406 g, 2.0 mmol), 5-acetoxy isophthaloyl chloride (117) (0.522 g, 2.0 mmol), a catalytic amount of 1,4-diazabicyclo[2.2.2]octane, and a catalytic amount of potassium iodide in 20 mL of pyridine was brought to 50° C. while stirring under nitrogen. After 24 hours, butanediol (0.072 g, 0.8 mmol) diluted in 10 mL of pyridine was added to the reaction mixture using a syringe pump over 8 hours. The solution was then quenched in 200 mL of cold 1N hydrochloric acid. The polymer precipitate is collected by filtration, redissolved in tetrahydrofuran, and precipitated in 100 mL of cold 1N hydrochloric acid. The polymer is then collected by filtration and dried under high vacuum. The polymer was found to have a molecular weight of ˜12,000 g/mol by GPC.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895691B2
出典データセットuspto-grants-2014_11
ORD IDord-e5e170c0b4a14c0d89717d6da1f7eab3
出典メモuspto-grants-2014_11