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HRID 1962214作成日:2026年10月27日

Boron trifluoride etherate → 3-Cyclopentyl-2-methoxy-3-oxo-propionic acid methyl ester

https://huagongshe.com/reaction/1962214

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物Ethyl 3-cyclopentyl-3-oxopropanoateHCID 11159709—
反応物Acetic acid;iodosylbenzeneHCID 73357407—
溶媒MethanolHCID 887—
生成物3-Cyclopentyl-2-methoxy-3-oxo-propionic acid methyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415366B2
出典データセットuspto-grants-2013_04
ORD IDord-ad24e586c5144c8b9edf1c2ab1625b27
出典メモuspto-grants-2013_04