HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903855Generated: October 31, 2026
Benzene, 1-bromo-3-(trifluoromethyl)- → HCID 23335287, compound
https://huagongshe.com/reaction/903855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene, 1-bromo-3-(trifluoromethyl)- | HCID 9817 | — |
| Reactant | 2-Methyl-5-hydroxypyridine | HCID 14275 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23335287 | HCID 23335287 | — |
Reaction Steps
3.68 g of a potassium salt of 5-hydroxy-2-methylpyridine was suspended in 10 ml of dimethylformamide, and 5.65 g of m-bromobenzotrifluoride and 300 mg of copper powders were added to the suspension, followed by allowing the mixture to react in a nitrogen stream at 120° C. for 15 hours while stirring. After cooling, the reaction mixture was diluted with 40 ml of acetone and filtered. The filtrate was immediately dried to solidify, and 100 ml of chloroform and 50 ml of water were added thereto. The mixture was adjusted to a pH of 9 with 5 N sodium hydroxide, and any insoluble matter was again separated by filtration. The resulting chloroform layer was dried with anhydrous sodium sulfate and immediately concentrated to dryness to obtain 4.1 g of oily 5-(m-trifluoromethylphenoxy)-2-methylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04229448 |
|---|
| Source dataset | uspto-grants-1980_10 |
|---|
| ORD ID | ord-7575242b326e478c8403a225747e6fa5 |
|---|
| Source note | uspto-grants-1980_10 |
|---|