HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 10398395, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 10085050 | HCID 10085050 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 10398395 | HCID 10398395 | 50.4% |
Reaction Steps
A solution of 10.8 g of methyl 2,3-epoxy-3-(4-methylphenyl)-5,5-dimethoxypentanoate and 1.1 g of p-toluenesulfonic acid in 60 ml of anhydrous benzene is refluxed over molecular sieves for 3 h. 60 ml of ethyl acetate are added, the mixture is washed 2 times with 50 ml of a NaHCO3 saturated aqueous solution, dried over Na2SO4 and the solvent is evaporated under reduced pressure. The residue is purified by F.C. to obtain 4.2 g of a yellow oil (50% yield). 1H NMR (CDCl3), δ: 2.39 (s, 3 H), 3.85 (s, 3 H), 6.62 (d, 1 H), 7.24 (d, 2 H), 7.48 (d, 2 H), 7.56 (d, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05538987 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-f5341716119c4fbda643e32458c76f68 |
| Source note | uspto-grants-1996_07 |