HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 86596759, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(Dimethoxymethyl)-2,4-dimethoxybenzene | HCID 14287325 | — |
| Reactant | HCID 22137749 | HCID 22137749 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 86596759 | HCID 86596759 | 74% |
Reaction Steps
A hot solution of 6.6 g N-(2-nitrobenzenesulfenyl)-3-phenylisoserine in 100 ml of dry benzene is added with 0.5 g of pyridinium p-toluenesulfonate and 5.3 g of 2,4-dimethoxybenzaldehyde dimethylacetal. The solution is refluxed for 4 hours, then left to cool to room temperature. After that, 10 ml of a NaHCO3 saturated solution are added and the phases are separated. The aqueous phase is extracted with ethyl acetate and the combined organic phases are dried over Na2SO4 and evaporated under reduced pressure. The residual yellow oil is purified by chromatography (silica,hexane-ethyl acetate 5:1 with 2% triethylamine) to give the desired product in 74% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053222B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-46d723a0ac1c40b2a60a4de374268db4 |
| Source note | uspto-grants-2006_05 |