HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → alpha-Trifluoromethyl-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-(4-Chlorophenyl)-3-methylbutanoyl chloride | HCID 4178001 | — |
| Reactant | 2,2,2-Trifluoro-1-(3-phenoxyphenyl)ethan-1-ol | HCID 14270571 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | alpha-Trifluoromethyl-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoate | HCID 53818390 | 98.3% |
Reaction Steps
This compound was prepared in the manner of Example II, using 5.3 g of 2-(4-chlorophenyl)-3-methylbutanoyl chloride, whose preparation is described in Agr. Biol. Chem., 38, 881 (1974), together with J. Kagaku To Seibutsu, 14, 427 (1976), 4.6 g of α-trifluoromethyl-3-phenoxybenzyl alcohol, and 1.5 g of pyridine in 50 ml of toluene. Volatiles were removed from the crude reaction product at 100° C./0.02 mm through a short path Kugelrohr distillation system to give as a residue 7.8 g of α-trifluoromethyl-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoate. The ir spectrum was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04152455 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-2168c1c5860e41bcbe412bf4e1bd93fc |
| Source note | uspto-grants-1979_05 |