HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 131723764, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | 1,3-Dithiolane, 2-pentyl- | HCID 9834108 | — |
| Reactant | HCID 12070523 | HCID 12070523 | — |
| Reactant | HCID 57035733 | HCID 57035733 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 131723764 | HCID 131723764 | — |
Reaction Steps
Into a 300 ml rocking autoclave were charged 58.2 g (0.331 m) of 2-(n-pentyl)-1,3-dithiolane, 1.06 g of sulfur, 0.12 g of p-toluenesulfonic acid, and 1.87 g of cobalt polysulfide catalyst (added as a 43% slurry in toluene). The autoclave was pressurized with hydrogen and maintained between 1600 and 2200 psi while being heated to 250°. After cooling and venting, the crude product contained 57% of the hydrogenolysis product, CH3(CH2)5S(CH2)2SH, as determined by GC/MS. When this procedure is applied to the product of Example 1, the hydrogenolysis product, (MeO)3Si(CH2)3S(CH2)2SH, is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518335B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-0bb27f2e35774abea7c25de39fa783bf |
| Source note | uspto-grants-2003_02 |