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化工社化工社 化学情報印刷レポート · 研究参考用
HRID 748662作成日:2026年10月27日

Ethanol → Dimethyl Sulfide

https://huagongshe.com/reaction/748662

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物MethanethiolHCID 878—
反応物MethanolHCID 887—
反応物EthanethiolHCID 6343—
反応物SulfurHCID 5362487—
生成物Dimethyl SulfideHCID 1068—
生成物Ethyl sulfideHCID 9609—
生成物Ethyl methyl sulfideHCID 12230—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07399893B2
出典データセットuspto-grants-2008_07
ORD IDord-d4465cdf039543f1bbf379bcdc8b34c4
出典メモuspto-grants-2008_07