化工社化工社 化学情報印刷レポート · 研究参考用
Imidazole → (Tert-butyl-dimethyl-silanyloxy)-cyclopropyl-acetic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 反応物 | Methyl cyclopropyl(hydroxy)acetate | HCID 11073449 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (Tert-butyl-dimethyl-silanyloxy)-cyclopropyl-acetic acid methyl ester | HCID 86711764 | — |
反応手順
To a solution of cyclopropyl-hydroxy-acetic acid methyl ester (1.00 g, 7.68 mmol) in DCM (9 mL) was added tert-butyldimethylsilyl chloride (1.27 g, 8.45 mmol) and imidazole (628 mg, 9.22 mmol). The reaction mixture was stirred at RT for 65 hours before being quenched with water (10 mL) and 1M HCl (5 mL). The mixture was extracted with ethyl acetate (3×15 mL) and the combined organic phases were washed with 1M HCl (10 mL), brine (10 mL), dried (Na2SO4) then concentrated in vacuo. This gave (tert-Butyl-dimethyl-silanyloxy)-cyclopropyl-acetic acid methyl ester as an amber oil (1.66 g, 88%). 1H NMR (400 MHz, CDCl3): δ 3.81 (1H, d, J=6.33 Hz), 3.74 (3H, s), 1.23-1.13 (1H, m), 0.89 (9H, s), 0.52-0.0.38 (4H, m), 0.06 (3H, s), 0.04 (3H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09346817B2 |
| 出典データセット | uspto-grants-2016_05 |
| ORD ID | ord-aa50b66a045e434a8d9f13d1feb4dc36 |
| 出典メモ | uspto-grants-2016_05 |