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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059046Generated: November 4, 2026

p-Toluenesulfonic acid → HCID 131723764, compound

https://huagongshe.com/reaction/1059046

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSulfurHCID 5362487—
Reactant1,3-Dithiolane, 2-pentyl-HCID 9834108—
ReactantHCID 12070523HCID 12070523—
ReactantHCID 57035733HCID 57035733—
ReactantHCID 178418361HCID 178418361—
SolventTolueneHCID 1140—
ProductHCID 131723764HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518335B2
Source datasetuspto-grants-2003_02
ORD IDord-0bb27f2e35774abea7c25de39fa783bf
Source noteuspto-grants-2003_02