関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Isophthaloyl chloride | HCID 7451 | — |
| 反応物 | Dabco | HCID 9237 | — |
| 反応物 | Butanediol | HCID 165788 | — |
| 反応物 | 3-Hexene-2,5-diol | HCID 5363299 | — |
| 反応物 | 1,3-Benzenedicarbonyl dichloride, 5-(acetyloxy)- | HCID 10515530 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | (E)-Hex-3-ene-2,5-diol isophthaloyl chloride 5-acetoxy isophthaloyl chloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08895691B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-e5e170c0b4a14c0d89717d6da1f7eab3 |
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| 出典メモ | uspto-grants-2014_11 |
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