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HRID 590755作成日:2026年10月25日

Hydrogen Peroxide → 5-(Prop-2-en-1-yl)cyclopent-2-en-1-one

https://huagongshe.com/reaction/590755

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Ammonium ChlorideHCID 25517—
反応物2-Allyl-5-(phenylselanyl)cyclopentanoneHCID 86665794—
溶媒DichloromethaneHCID 6344—
生成物5-(Prop-2-en-1-yl)cyclopent-2-en-1-oneHCID 13444545—

反応手順

A stirred, ice cold (3° C.) solution of 2-allyl-5-(phenylselanyl)cyclopentanone, mixture of isomers (12.0 g, 43 mmol) in dichloromethane (200 mL) in a 1 L round bottomed-flask equipped for boil-over containment was treated with saturated aqueous ammonium chloride (45 mL), then dropwise with 30% aqueous hydrogen peroxide (22 mL), and slowly carefully warmed to room temperature. At approximately 20° C. a vigorous exotherm started, and the ice bath was re-applied. The mixture was cooled to room temperature and stirred for 1 h, then the solution was washed with water (100 mL), stirred with 10% aqueous sodium thiosulfate pentahydrate (75 mL) for 10 min, and separated. The organic solution was washed with saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride (75 mL each), dried (Na2SO4), and concentrated to 30 mL volume. The solution was added to a silica gel column (˜400 cc) and eluted with dichloromethane to afford (after very gentle concentration of appropriate fractions) 5-allylcyclopent-2-enone (3.95 g, 75%) as a very pale yellow oil. NMR (CDCl3): δ 7.61 (m, 1 H), 6.12 (m, 1 H), 5.60-5.75 (m, 1 H), 4.90-5.05 (m, 2 H), 2.70-2.80 (m, 1H), 2.45-2.55 (m, 1 H), 2.30-2.40 (m, 2 H), 2.05-2.15 (m, 1 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09233985B2
出典データセットuspto-grants-2016_01
ORD IDord-52199717abc844939a213d3c3d8a9ffd
出典メモuspto-grants-2016_01