HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dimethylpyridine → 2-Chloro-5-[Bis-(4-Chlorophenyl)-Methyl]-Pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dimethylpyridine | HCID 7936 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 5-[Bis-(4-Chlorophenyl)-Methyl]-2-Pyridone | HCID 22748768 | — |
| Product | 2-Chloro-5-[Bis-(4-Chlorophenyl)-Methyl]-Pyridine | HCID 22748777 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To a mixture of 35.2 g. (0.11 mole) of 5-[bis-(4-chlorophenyl)-methyl]-2-pyridone and 11.8 g. (0.11 mole) of 2,4-lutidine, add 50.6 g. (0.33 mole) of phosphorous oxychloride (dropwise) while heating the reaction mixture at 80°. Then, heat the reaction mixture at 120° C. for six hours. Pour the reaction mixture onto ice, basify with ammonium hydroxide, extract with benzene and remove both the benzene and residual 2,4-lutidine by distillation. Distill the residue at about 195°-210° C. (0.01 mm) to obtain thereby about 30 g. of the product of this step as a yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04138488 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-811dd63dab5743bb80fa0d1a1b9160cf |
| Source note | uspto-grants-1979_02 |