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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 748662생성일: 2026년 10월 26일

Ethanol → Dimethyl Sulfide

https://huagongshe.com/reaction/748662

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물MethanethiolHCID 878—
반응물MethanolHCID 887—
반응물EthanethiolHCID 6343—
반응물SulfurHCID 5362487—
생성물Dimethyl SulfideHCID 1068—
생성물Ethyl sulfideHCID 9609—
생성물Ethyl methyl sulfideHCID 12230—

반응 단계

To produce a sulfide, the sulfur compound reactant stream 10b can be a mercaptan, such as methanethiol (methyl mercaptan) or ethanethiol (ethyl mercaptan). Either one of these mercaptans can be reacted with methanol or ethanol as the alcohol feed stream 8b to produce 2-thiopropane (dimethyl sulfide), 1-(methylthio)ethane (methyl ethyl sulfide), or 1,1′-thiobisethane (diethyl sulfide), depending upon the selected sulfur compound reactant stream 10b and alcohol feed stream 8b. For example, methanethiol (methyl mercaptan) can be reacted with methanol, in the presence of the catalyst blend 5b of the present invention, to produce 2-thiopropane (dimethyl sulfide) or with ethanol to produce 1-(methylthio)ethane (methyl ethyl sulfide). As another example, ethanethiol (ethyl mercaptan) can be reacted with methanol to produce 1-(methylthio)ethane (methyl ethyl sulfide) or with ethanol to produce 1,1′-thiobisethane (diethyl sulfide). As shown in FIG. 3, the catalyst blend 5b includes a plurality of zones with each zone having a lower volumetric ratio of the alumina diluent B to the hydrotreating catalyst A than the previous zone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07399893B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-d4465cdf039543f1bbf379bcdc8b34c4
출처 메모uspto-grants-2008_07