反応式
[S].[CH3:2][SH:3].[CH2:4]([SH:6])[CH3:5].CO.[CH2:9](O)[CH3:10]>>[CH3:9][S:6][CH3:4].[CH3:2][S:3][CH2:4][CH3:5].[S:6]([CH2:9][CH3:10])[CH2:4][CH3:5]参加物
実験手順
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.
出典と根拠
- ORDレコード
- ord-d4465cdf039543f1bbf379bcdc8b34c4
- 出典データセット
- uspto-grants-2008_07
- 特許番号
- US07399893B2
関連ノート
読み込み中…