化工社化工社 化学情報印刷レポート · 研究参考用
Tetrahydrofuran → 6-(2-Hydroxy-ethyl)-2,5,7-trimethyl-2-triethylsilanyloxymethyl-indan-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | CID 15879360 | HCID 15879360 | — |
| 反応物 | 2,5,7-Trimethyl-2-triethylsilanyloxymethyl-6-vinyl-indan-1-ol | HCID 68475157 | — |
| 生成物 | 6-(2-Hydroxy-ethyl)-2,5,7-trimethyl-2-triethylsilanyloxymethyl-indan-1-ol | HCID 68473560 | 81% |
反応手順
To the stirred solution of compound 8 (0.85 g, 2.45 mmol) in dry THF was added (Cy)2BH (0.87 g, 4.91 mmol) slowly at 0° C. under argon atmosphere. The reaction mixture was warmed to room temperature and stirred for 12 h. The reaction mixture was quenched with 2N NaOH (6 mL) and H2O2 (3 mL) at 0° C. and allowed to stir for 4 h. Then crude reaction mixture was extracted with ethyl acetate (40 mL), washed with water (10 mL), brine (10 mL) dried (Na2SO4) and concentrated in vacuo. Purification by column chromatography (SiO2, 8 to 10% EtOAc in petroleum ether eluant) gave pure compound 9 (0.72 g, 81%) as gummy syrup.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08633252B2 |
| 出典データセット | uspto-grants-2014_01 |
| ORD ID | ord-ffcdd68e47104200a9b3c4395ec2e520 |
| 出典メモ | uspto-grants-2014_01 |