Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | HCID 21419830 | HCID 21419830 | — |
| Reactant | Methylorthoformate | HCID 53629101 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68124295 | HCID 68124295 | 69% |
Reaction Steps
16.5 g of methyl orthoformate were added to a solution of 27.6 g of m-valeramido-acetylacetanilide in 50 ml of methanol and after the addition of 0.5 g of p-toluene sulfonic acid, the mixture was stirred for 72 hours at 20° C. 200 ml of toluene and 1 ml of quinoline were added and the mixture was heated at 140° C. for 1 hour while distilling a methanol-toluene azeotrope. The mixture was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with an 8- 2 methylene chloride-acetone mixture yielded 20 g of m-valeramido-3-methoxy-crotonanilide melting at 115° C. and after crystallization from ethyl acetate melted at 116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04039316 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-774bf5c3f37d4c8e856e32775a974227 |
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| Source note | uspto-grants-1977_08 |
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