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HRID 1763073作成日:2026年10月26日

1,3-Dichloro-2-butene → 6,7-Dichloro-2-(3-chloro-2-butenyl)-2,3-dihydro-5-methoxy-2-propyl-1H-inden-1-one

https://huagongshe.com/reaction/1763073

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Dichloro-2-buteneHCID 13556—
反応物Sodium hydrideHCID 24758—
反応物6,7-Dichloro-2,3-dihydro-5-methoxy-2-propyl-1H-inden-1-oneHCID 13613323—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物6,7-Dichloro-2-(3-chloro-2-butenyl)-2,3-dihydro-5-methoxy-2-propyl-1H-inden-1-oneHCID 5379214380.2%

反応条件

温度30 °C

反応手順

6,7-Dichloro-2,3-dihydro-5-methoxy-2-propyl-1H-inden-1-one (13.66 g, 0.05 mole) dissolved in toluene (80 ml) was added over 15 minutes with stirring under N2 to a suspension of 56% sodium hydride (2.36 g, 0.055M) in dimethylformamide (65 ml) and toluene (15 ml) at 25°. The mixture was stirred without external heat for 11/2 hours, at 50° C. for 1/2 hour and then cooled to 30° C. A solution of 1,3-dichloro-2-butene (7.81 g, 0.0625 mole) in toluene (10 ml) was added, and the mixture was heated at 50°-55° for 2 hours, poured into ice water, and extracted with diethyl ether. The organic extracts were washed with water, dried over MgSO4, concentrated under vacuum and chromatographed on silica with elution with 1/1 hexane/methylene chloride to obtain 14.5 g of product as an oil which was a mixture of cis-trans isomers.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04835313
出典データセットuspto-grants-1989_05
ORD IDord-e6daa8aa740140448fb4d4196252b91b
出典メモuspto-grants-1989_05