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HRID 28728作成日:2026年10月25日

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

https://huagongshe.com/reaction/28728

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US07419994B2
出典データセットuspto-grants-2008_09
ORD IDord-23a373f342e84df88f508be7b6bf9eea
出典メモuspto-grants-2008_09