化工社化工社 化学情報印刷レポート · 研究参考用
tert-Butanol → 1-(2,3-Dihydroxy-propyl)-cyclohexane-1,3-dicarboxylic acid diethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | tert-Butanol | HCID 6386 | — |
| 反応物 | Quinuclidine | HCID 7527 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Sodium Sulfite | HCID 24437 | — |
| 反応物 | 1-Allyl-cyclohexane-1,3-dicarboxylic acid diethyl ester | HCID 67108610 | — |
| 触媒 | HCID 178511488 | HCID 178511488 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-(2,3-Dihydroxy-propyl)-cyclohexane-1,3-dicarboxylic acid diethyl ester | HCID 67108500 | — |
反応手順
To a solution of 1-allyl-cyclohexane-1,3-dicarboxylic acid diethyl ester from step 2 (250 g, 0.93 mol) in t-butanol (2.3 L) and water (2.3 L) was added potassium ferricyanide (920 g, 2.79 mol), potassium carbonate (386 g, 2.79 mol), potassium osmate dihydrate (4.75 g, 13 mmol) and quinuclidine (0.073 g, 7.0 mmol). The resulting dark colored solution was stirred at rt overnight and then quenched with portion-wise addition of sodium sulfite (1.05 kg, 8.37 mol). After dilution with ethyl acetate, it was extracted, washed with water and brine, dried over Na2SO4, and concentrated under reduced pressure. The resulting residue (224 g) was used in the next step without delay and without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08633190B2 |
| 出典データセット | uspto-grants-2014_01 |
| ORD ID | ord-7468b90972ee44d690b9f8ca57c7a586 |
| 出典メモ | uspto-grants-2014_01 |