戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1978246作成日:2026年10月24日

Isopropanol → 1-Isopropoxycyclohexene

https://huagongshe.com/ja/reaction/1978246

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物CyclohexanoneHCID 7967—
反応物Propane, 2,2',2''-[methylidynetris(oxy)]tris-HCID 78191—
反応物Sodium bisulfate monohydrateHCID 23673662—
生成物1-IsopropoxycyclohexeneHCID 436613681.7%

反応条件

温度60 °C

反応手順

To a mixture at room temperature containing 196.32 grams (2 mol) of cyclohexanone, 390.4 grams (2.06 mol) of triisopropyl orthoformate and 12.00 grams of isopropanol (0.2 mol), was added 7.6 grams (0.055 mol) of sodium hydrogensulfate monohydrate. The reaction was exothermic and upon addition of the catalyst, the temperature of the reaction mixture rose to 35° C., and was heated and maintained at 60° C. for 1 hour. The progress of the reaction was monitored by GC until the cyclohexanone content dropped to less than 2%. The isopropanol and isopropyl formate were distilled off under reduced pressure until the reaction mixture's temperature reached a maximum of 100° C. The reaction mixture was cooled to room temperature and filtered to remove sodium hydrogensulfate monohydrate (recovered). The pH value of the filtrate was adjusted to about 7˜8 by adding 0.8 gram of potassium iso-propoxide. The mixture was then heated under reduced pressure to remove unreacted cyclohexanone. The product, 1-isopropoxy-1-cyclohexene was isolated by distillation as a clear liquid; the yield was 81.7% with a purity exceeding 98%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06235944B1
出典データセットuspto-grants-2001_05
ORD IDord-d286ee6461874790a52c5b142e85ede8
出典メモuspto-grants-2001_05