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HRID 256207作成日:2026年10月25日

Ethylene Glycol → 1-(3',4'-Dimethoxyphenyl)-7-(4'-chlorophenyl)-2-nitro-5-heptanone ethylene ketal

https://huagongshe.com/reaction/256207

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物p-Toluenesulfonic acidHCID 6101—
反応物1-(3',4'-Dimethoxyphenyl)-7-(4'-chlorophenyl)-2-nitro-5-heptanoneHCID 20164188—
溶媒CyclohexaneHCID 8078—
生成物1-(3',4'-Dimethoxyphenyl)-7-(4'-chlorophenyl)-2-nitro-5-heptanone ethylene ketalHCID 56638132—

反応手順

Into 1.1 r.b. flask equipped with a Dean Stark trap was placed 65 g (0.16 mole) of 1-(3',4'-dimethoxyphenyl)-7-(4'-chlorophenyl)-2-nitro-5-heptanone, 2 g p-toluenesulfonic acid, 100 ml ethylene glycol and 400 ml of cyclohexane. The mixture was allowed to reflux overnight, then concentrated in vacuo. Dil NaHCO3 solution was added to the residue and extracted with methylene chloride. The organic layer was backwashed with water, dried over anh MgSO4, filtered and concentrated under reduced pressure to obtain 45.3 g of an oil which solidified on drying at room temperature under vacuum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04701461
出典データセットuspto-grants-1987_10
ORD IDord-9fd003e37b4d4e8787dc4ae5969a3dff
出典メモuspto-grants-1987_10