HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 4-(Chlorodiphenylmethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | alpha,alpha-Diphenyl-4-pyridinemethanol | HCID 74177 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-(Chlorodiphenylmethyl)pyridine | HCID 13215895 | — |
Reaction Steps
92.1 g (0.353 mol) of diphenyl(4-pyridyl)methyl alcohol recrystallized from chloroform and 800 ml of simple-distillation benzene were charged in a 2-l three-necked flask provided with a stirrer and reflux condenser. The mixture was treated at 50° C. to form a suspension. 29.6 ml (0.407 mol) of thionyl chloride was poured in the suspension and the mixture was stirred under reflux for 1 h. The resulting solution was cooled to room temperature. 72.5 ml (0.522 mol) of triethylamine was added thereto and the mixture was stirred for 7 h. The reaction solution was filtered and the filtrate was concentrated to obtain crude diphenyl(4-pyridyl)methyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04473690 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-0e65485d873741038106db271a2c4286 |
| Source note | uspto-grants-1984_09 |