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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65800생성일: 2026년 10월 24일

Carbon Dioxide → 2,3,6-Trimethylphenol

https://huagongshe.com/ko/reaction/65800

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물2-Cyclohexen-1-one, 2,5,6-trimethyl-HCID 89264—
반응물2,3,6-Trimethylcyclohex-2-en-1-oneHCID 3016843—
반응물Trimethyl-2-cyclohexen-1-oneHCID 13360364—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
생성물2,3,6-TrimethylphenolHCID 1701695%

반응 단계

Dehydrogenation may be carried out in an inert solvent. It is advantageous however to dehydrogenate the 2,5,6-trimethyl-2-cyclohexen-1-one or 2,3,6-trimethyl-2-cyclohexen-1-one in the gas phase, for example by passing it as a gas at the dehydrogenation temperature over a palladium/silica gel catalyst. In gas-phase dehydrogenation the trimethyl-2-cyclohexen-1-one is preferably passed over the catalyst in admixture with an extraneous gas such as nitrogen, steam, carbon dioxide and particularly hydrogen; generally a ratio by volume of extraneous gas to gaseous trimethyl-2-cyclohexen-1-one of from about 1:2 to 5:1 is chosen. Temperatures of from 200° to 400° C., preferably from 250° to 350° C., are usually used in gas-phase dehydrogenation. The time that the trimethyl-2-cyclohexen-1-one is in contact with the catalyst is generally from half to fifty, preferably from two to ten seconds. The 2,3,6-trimethylphenol is obtained in a more than 95% yield in gas-phase dehydrogenation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04128728
출처 데이터셋uspto-grants-1978_12
ORD IDord-4aab1458444845a2a8ad075eb5623b03
출처 메모uspto-grants-1978_12