関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bis(2-bromoethyl) ether | HCID 21521 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | (3-Methoxyphenyl)acetonitrile | HCID 88310 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 4-(3-Methoxyphenyl)oxane-4-carbonitrile | HCID 18786366 | 93.5% |
反応手順
A mixture of NaH (3.2 g, 79 mmol) in 50 mL NMP stirred at 0° C., was treated dropwise with a mixture of 2-(3-methoxyphenyl)acetonitrile (3.9 g, 26 mmol) and 1-bromo-2-(2-bromoethoxy)ethane (6.1 g, 26 mmol) in 20 mL. The mixture was allowed to warm to room temperature and stirred for 15 hours, M+1=218. The mixture was then carefully quenched with 100 mL H2O and the pH was adjusted to 5. The mixture was extracted with ether (3×100 mL). The combined organic layers were washed with H2O (3×50 mL) and brine (20 mL). The organic layer was dried over anhydrous Na2SO4, concentrated in vacuo, and purified by column chromatography eluting with 10-20% EtOAc/hexane to give 5.28 g of the crude product 5.28 g as a pale yellow oil. MS (m/z)=218 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07635715B2 |
|---|
| 出典データセット | uspto-grants-2009_12 |
|---|
| ORD ID | ord-b3c61d16b4bf41a7a9fc7033fef635f9 |
|---|
| 出典メモ | uspto-grants-2009_12 |
|---|