HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Trifop-methyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Trifop | HCID 181206 | — |
| Solvent | Water | HCID 962 | — |
| Product | Trifop-methyl | HCID 94586 | 74% |
Reaction Steps
10 g of α-[4-(4-trifluoromethylphenoxy)phenoxy]propionic acid was reacted with 80 g of methanol in the presence of 5 g of boron trifluoride at 55° to 60° C. for 3 hours. The reaction product was poured into water, and extracted with chloroform. The extract was washed with dilute alkali (i.e., 2-3% NaOH aqueous solution) and water, and dried. Then, the chloroform was evaporated off. The residue was distilled at reduced pressure to afford 7.5 g of the final product having a boiling point of 165° to 167° C./3 mmHg. The yield was 74%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04314069 |
| Source dataset | uspto-grants-1982_02 |
| ORD ID | ord-db512bc3eae445afbc3c10506211120e |
| Source note | uspto-grants-1982_02 |