Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748662Generated: October 25, 2026

Ethanol → Dimethyl Sulfide

https://huagongshe.com/reaction/748662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethanethiolHCID 878—
ReactantMethanolHCID 887—
ReactantEthanethiolHCID 6343—
ReactantSulfurHCID 5362487—
ProductDimethyl SulfideHCID 1068—
ProductEthyl sulfideHCID 9609—
ProductEthyl methyl sulfideHCID 12230—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399893B2
Source datasetuspto-grants-2008_07
ORD IDord-d4465cdf039543f1bbf379bcdc8b34c4
Source noteuspto-grants-2008_07