HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → Acetonitrile, [[4-[(4-methoxyphenyl)amino]-6-methyl-2-pyrimidinyl]thio]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Acetonitrile, [(4-chloro-6-methyl-2-pyrimidinyl)thio]- | HCID 12228966 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Acetonitrile, [[4-[(4-methoxyphenyl)amino]-6-methyl-2-pyrimidinyl]thio]- | HCID 12228969 | — |
Reaction Steps
A stirred mixture of 15.0 g. (0.075 mole) of (4-chloro-6methyl-2-pyrimidinylthio)aceto nitrile, 10.0g. (0.075 mole) p-anisidine and 7.5 g. (0.075 mole) of sodium carbonate in 150 ml of ethanol was heated under reflux for five hours. The mixture was filtered and the filtrate was evaporated in a rotary evaporator. The oily residue was dissolved in ethyl acetate. Dilution of the ethyl acetate solution with petroleum ether and cooling in ice yielded a precipitate. This solid was collected and recrystallized from a mixture of benzene-petroleum ether to afford 7.2 g. of product, m.p. 128°-131°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03950339 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-e29539e88d2246e2adbe451d183be3ad |
| Source note | uspto-grants-1976_04 |