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HRID 61337생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methanesulfonic AcidHCID 6395—
반응물Trimethyl orthoformateHCID 9005—
반응물Methallyl alcoholHCID 10557—
반응물2,6-DimethylcyclohexanoneHCID 17780—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물2,6-Dimethyl-2-(2-methyl-allyl)-cyclohexanoneHCID 89705189—

반응 조건

온도60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09441185B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-f861df3ab22d4c698f270ecab7903ace
출처 메모uspto-grants-2016_09