HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrothiophene → Hydrogen Sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrothiophene | HCID 1127 | — |
| Reactant | Butanethiol | HCID 8012 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Product | Hydrogen Sulfide | HCID 402 | — |
| Product | 2,4,4-Trimethyl-1-pentene | HCID 7868 | — |
| Product | 1-Octanethiol | HCID 8144 | — |
Reaction Steps
Thiophene hydrodesulfurization proceeds in the first reactor. Because a catalyst with low hydrogenation activity was used, no thiacyclopentane or butylthiol production was found in the thiophene hydrogenation product. Octylthiol was also produced by reaction between diisobutylene and hydrogen sulfide generated by the hydrodesulfurization. In the second reactor, the octylthiol produced by the first reactor was hydrodesulfurized, yielding a model gasoline base with a total sulfur content of no greater than 10 ppm by weight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08303805B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-e50dcea785a74c798fdc9732f3598bbf |
| Source note | uspto-grants-2012_11 |