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HRID 61337作成日:2026年10月23日

Hydrochloric Acid → 2,6-Dimethyl-2-(2-methyl-allyl)-cyclohexanone

https://huagongshe.com/ja/reaction/61337

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Methanesulfonic AcidHCID 6395—
反応物Trimethyl orthoformateHCID 9005—
反応物Methallyl alcoholHCID 10557—
反応物2,6-DimethylcyclohexanoneHCID 17780—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物2,6-Dimethyl-2-(2-methyl-allyl)-cyclohexanoneHCID 89705189—

反応条件

温度60 °C

反応手順

2,6-Dimethyl-cyclohexanone (1 kg, 4 mol), trimethyl orthoformate (TMOF, 880 g), and methanol (800 mL) were charged to a 5 L reaction flask. HCl was added quickly. Reaction exothermed and the temperature increased from 14° C. to 20° C. The reaction mixture was heated to 60° C. and aged for 7 hours. When the reaction was about 75% complete, the reaction mixture was quenched with NaOCH3 (25%, 25 g), heated to 90° C., and applied to a Bidwell-Sterling trap. The reaction mixture was then cooled to room temperature followed by sequential addition of methallyl alcohol (1.25 Kg, 8.5 moles), HOAc (50 g), and methane sulfonic acid (MSA, 10 g). The resulting mixture was heated to 110° C., applied to a Bidwell-Sterling trap, and aged for 4 hours until gas chromatograph analysis indicated that the reaction was 95% completed. The reaction mixture was then cooled and washed with saturated sodium carbonate solution (3 L) to provide the crude product 2,6-dimethyl-2-(2-methyl-allyl)-cyclohexanone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09441185B2
出典データセットuspto-grants-2016_09
ORD IDord-f861df3ab22d4c698f270ecab7903ace
出典メモuspto-grants-2016_09