HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → Ethyl 2-methyl-4-phenylpyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | Ethyl 2-methyl-4-phenyl-1,4-dihydropyridine-3-carboxylate | HCID 14652661 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-methyl-4-phenylpyridine-3-carboxylate | HCID 14652662 | 79.9% |
Reaction Steps
To a solution of 0.32 mol ethyl 1,4-dihydro-2-methyl-4-phenyl-3-pyridinecarboxylate in 50 ml of methylene chloride was added 16 g (0.5 mol) of sulfur. The temperature of the well-stirred dark solution was raised over a period of about 30 minutes to 170°-180° C. When the development of hydrogen sulfide had subsided, the reaction mixture was cooled to room temperature, taken up in toluene, and filtered through Celite filter aid. The filtrate was concentrated under vacuum and the residue chromatographed on silica gel, eluting with ethyl acetate/hexane to yield 61.7 g of ethyl 2-methyl-4-phenyl-3-pyridinecarboxylate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04997837 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-6ad911ec9a6f485eacf6cbc181a1f886 |
| Source note | uspto-grants-1991_03 |