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HRID 9269作成日:2026年10月26日

Ethyl vinyl ether → 1-Bromo-5-vinyloxy-cyclopentene

https://huagongshe.com/reaction/9269

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl vinyl etherHCID 8023—
反応物2-Bromo-cyclopent-2-enolHCID 11137462—
触媒DiacetyloxymercuryHCID 16683746—
生成物1-Bromo-5-vinyloxy-cyclopenteneHCID 21986113—

反応手順

A solution of 2-bromo-cyclopent-2-enol (Intermediate D3) (21.7 g, 133.1 mmol) in ethyl vinyl ether (300 mL) was treated with Hg(OAc)2 (31.8 g, 99 mmol) at rt for 60 h. The mixture was quenched with 5% NaOH (150 mL) and filtered through celite. The residue was concentrated to yield 1-bromo-5-vinyloxy-cyclopentene as a pale yellow oil, 14.2 g (46%). 1-Bromo-5-vinyloxy-cyclopentene (14.1 g, 74.4 mmol) in toluene was heated in a re-sealable tube at 130° C. for 24 h. (2-Bromo-cyclopent-2-enyl)-acetaldehyde (Intermediate ONE 1) was isolated after flash chromatography on silica gel with hexanes to 5% ethyl acetate:hexanes, 10.4 g (74%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091232B2
出典データセットuspto-grants-2006_08
ORD IDord-34d736d2a0ea4ad099e56c5998df35eb
出典メモuspto-grants-2006_08