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HRID 42729作成日:2026年10月25日

Pyridine → 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime

https://huagongshe.com/reaction/42729

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物O-Methylhydroxylamine hydrochlorideHCID 521874—
反応物1-(2,2,4-Trimethyl-3-cyclohexen-1-yl)ethan-1-oneHCID 3016988—
溶媒MethanolHCID 887—
生成物1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oximeHCID 8667533892.4%

反応条件

温度24 °C

反応手順

To a stirred solution of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone (162 g; 0.97 mol), prepared as described in example P4, in methanol (500 ml) was added pyridine (160 ml; 1.95 mol) followed by a portionwise addition of methoxyamine hydrochloride (142 g; 1.70 mol). The reaction mixture was stirred at 24° C. for 16 hours under nitrogen atmosphere. Methanol was removed under reduced pressure, the residue poured in water (600 ml) and 1N hydrochloric acid was added (100 ml). The solution was extracted with dichloromethane (3×300 ml). Combined organic layers were washed with brine (500 ml) and dried over sodium sulfate. The solvent was removed in vacuo to afford 175 g (92% of theory) of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime as a clear red oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536215B2
出典データセットuspto-grants-2013_09
ORD IDord-949bef1b62f54a69bbcb37a365ea0c46
出典メモuspto-grants-2013_09