HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → n-Butyl 1-(4-iodophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(4-Iodophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylic acid | HCID 13084115 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | n-Butyl 1-(4-iodophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylate | HCID 13084143 | 52% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To 50 ml of n-butanol, cooled to -5° C., there is added dropwise 2.62 g (0.022 mol) of thionyl chloride. The solution is stirred at 0° C. for 15 minutes and to it there is added 7.12 g (0.02 mol) of 1-(4-iodophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylic acid. (See Example 3) The suspension formed is stirred at room temperature for 3 days and to it there is added 150 ml of hexane. The suspension is stirred at room temperature for 2 days and is vacuum filtered. The filter cake (HCl salt of the desired product) is air dried and slurried in 150 ml of water for 3 hrs. The suspension is vacuum filtered to afford 4.25 g (52% yield) of product, mp 137°-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04661145 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-9c903cf691fe404f9b0bebfeb9f12377 |
| Source note | uspto-grants-1987_04 |