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HRID 560138作成日:2026年10月27日

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

https://huagongshe.com/reaction/560138

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 ONE1) 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US08063086B2
出典データセットuspto-grants-2011_11
ORD IDord-16c01cfedf364868a7bc6c45635c34b5
出典メモuspto-grants-2011_11