化工社化工社 化学情報印刷レポート · 研究参考用
Boron trifluoride etherate → 3-Cyclopentyl-2-methoxy-3-oxo-propionic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Boron trifluoride etherate | HCID 8000 | — |
| 反応物 | Ethyl 3-cyclopentyl-3-oxopropanoate | HCID 11159709 | — |
| 反応物 | Acetic acid;iodosylbenzene | HCID 73357407 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-Cyclopentyl-2-methoxy-3-oxo-propionic acid methyl ester | HCID 59777286 | — |
反応手順
The title compound was prepared using a method analogous to that described in Tetrahedron 1998, 44, 1603-1607: To a suspension of iodosobenzene diacetate (5.2 g, 16.3 mmol) in MeOH (40 mL) was added BF3.OEt2 (2.1 mL, 16.3 mmol). The resulting mixture was added to 3-cyclopentyl-3-oxo-propionic acid ethyl ester (3.0 g, 16.3 mmol) and stirred at rt overnight. The mixture was concentrated to half the total volume, quenched with satd. aq. NaHCO3, and extracted with CHCl3 (2×). The combined organic layers were dried and concentrated and the crude residue purified (EtOAc/hexanes) to yield a colorless oil (1.5 g, 43%). 1H NMR (MeOD): 4.4 (s, 1H), 3.8 (s, 3H), 3.5 (s, 3H), 3.3-3.2 (m, 1H), 1.9-1.5 (m, 8H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08415366B2 |
| 出典データセット | uspto-grants-2013_04 |
| ORD ID | ord-ad24e586c5144c8b9edf1c2ab1625b27 |
| 出典メモ | uspto-grants-2013_04 |