HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorobenzene → Ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-(4-(Trifluoromethyl)phenoxy)phenol | HCID 170230 | — |
| Reactant | Ethyl 3,4-dibromopentanoate | HCID 12922552 | — |
| Catalyst | N,N-Dibutyl-N-ethylbutan-1-aminium bromide | HCID 19043781 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate | HCID 156921 | 95.2% |
Reaction Steps
In a reactor, 15 g of chlorobenzene and 15 g of water were charged, and 12.7 g (0.05 mole) of 4-(4-trifluoromethylphenoxy)phenol, 15.8 g (0.055 mole) of ethyl 3,4-dibromopentanoate and 8.7 g (0.063 mole) of potassium carbonate and 0.3 g (0.001 mole) of tributylethylammonium bromide were added. They were refluxed for 6 hours to react them. The water phase was separated and the organic phase was washed with 5% hydrochloric acid and with water and then, chlorobenzene, ethyl 3,4-dibromopentanoate and low boiling by-products were distilled off at 100° C. under a reduced pressure (0.02-0.05 mmHg) to obtain 18.1 g of ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate (nD20 1.5175). The yield was 95.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04267317 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-66aa32489e3a4ccfb619f2bf43f8dfb5 |
| Source note | uspto-grants-1981_05 |