HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-Chloro-4-chloromethylbiphenyl → 2-[4-(4-Chlorophenyl)benzyloxy]-3,3,3-trifluoro-2-trifluoromethylpropionitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-Chloro-4-chloromethylbiphenyl | HCID 12773846 | — |
| Reactant | 2-Hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionitrile sodium salt | HCID 86735168 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[4-(4-Chlorophenyl)benzyloxy]-3,3,3-trifluoro-2-trifluoromethylpropionitrile | HCID 20314462 | — |
Reaction Steps
A solution of 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionitrile sodium salt (4.3 g.) and 4-(4-chlorophenyl)-benzyl chloride (4.7 g.) in dimethylformamide (25 ml.) is stirred at ambient temperature for 10 days, then diluted with water. During this reaction, 2-[4-(4-chlorophenyl)benzyloxy]-3,3,3-trifluoro-2-trifluoromethylpropionitrile is formed and is subsequently hydrolysed to the corresponding amide. The mixture is extracted with 1,2,2-trichloro-1,1,2-trifluoroethane, and the extract is dried with sodium sulphate, then evaporated. The residue is crystallised from cyclohexane to give 2-[4-(4-chlorophenyl)benzyloxy]-3,3,3-trifluoro-2-trifluoromethylpropionamide, m.p. 123°-124° C. (1.6 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055595 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-870e0a4859d441b59a63a61308d443be |
| Source note | uspto-grants-1977_10 |