関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 1-Benzyl-2,5-dihydropyrrole | HCID 561506 | — |
| 反応物 | HCID 178506676 | HCID 178506676 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Cyclohexane diethylether | HCID 21895417 | — |
| 生成物 | 1-Benzyl-4-phenyl-3-pyrrolidinol | HCID 12044053 | 76.3% |
反応手順
To a solution of 15.9 g (0.1 mol) of 1-benzyl-3-pyrroline, 12.0 g (0.12 mol) of 98% sulfuric acid, and 60.0 g of THF in a quartz round flask reactor, 45.6 g (0.20 mol) of (NH4)2S2O8 (ammonium peroxydisulfate produced by Mitsubishi Gas Chemical Industry Co., Ltd.) was added with stirring and allowed to react for 5 days at room temperature with irradiation by 500 W Xe lamps (UXL-500D xenon lamp produced by Ushio). 300 mL (0.30 mol) of 1 mol/L phenyllithium (PhLi) in cyclohexane-diethyl ether solution (produced by Kanto Chemical Co., Inc.) was continuously added to the reaction mixture and stirred for 5 hours at about 5° C. using an ice-bath. After completion, water was added to destroy excess PhLi at about 5° C. using an ice-bath. Acetone and diethyl ether were evaporated under reduced pressure, and extracted with toluene and water. After the solvent was evaporated under reduced pressure, 19.3 g of 1-benzyl-4-phenyl-3-pyrrolidinol (yield 76.3%) was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06130338 |
|---|
| 出典データセット | uspto-grants-2000_10 |
|---|
| ORD ID | ord-8ab590d5a6c34c8691c591d23268d7e4 |
|---|
| 出典メモ | uspto-grants-2000_10 |
|---|