HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 13203356, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,2-Butanedithiol | HCID 61829 | — |
| Reactant | 5-Hydroxyoctan-4-one | HCID 219794 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13203356 | HCID 13203356 | — |
Reaction Steps
Butyroin (12.2 g), butane-1,2-dithiol (14.4 g) and p-toluenesulfonic acid (0.5 g) were dissolved in toluene (50 g) and the solution refluxed under a Dean-Stark trap. It was worked up as in Example 3 to give 2-ethyl-2,3-dihydro-5,6-dipropyl-1,4-dithiin as a clear greenish liquid, boiling range 92°-105°/0.025 mm, yield 8.5 g (44%). NMR(CDCl3), 0.78-1.14 δ (overlapping triplets), 1.21-1.80 δ (multiplet) 2.07-2.37 δ (complex quartet), 2.6-3.4 δ (multiplet).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04319033 |
| Source dataset | uspto-grants-1982_03 |
| ORD ID | ord-825519268a4f44b19c0c0b6359dce350 |
| Source note | uspto-grants-1982_03 |