HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 21422772, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | HCID 21422770 | HCID 21422770 | — |
| Reactant | Methylorthoformate | HCID 53629101 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21422772 | HCID 21422772 | — |
Reaction Steps
A mixture of 23.5 g of m-(n-butylcarbamoyloxy)-acetylacetanilide 15 g of methyl orthoformate, 75 ml of methanol and 0.5 g of p-toluene sulfonic acid was stirred for 24 hours and 1 ml of quinoline was then added. The solvent was evaporated and the residue was chromatographed over silica. Elution with an 8-2 methylene chloride-acetone mixture yielded 20 g of m-(n-butylcarbamoyloxy)-3,3-dimethoxy-butyranilide melting at 114°C. STEP B: m-(n-butylcarbamoyloxy)-3-methoxy-crotonanilide
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04036633 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-f8f95645f26c4717a91ccde347cc68af |
| Source note | uspto-grants-1977_07 |