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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-bromo-3-(trifluoromethyl)-HCID 9817—
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
ReactantPotassiumHCID 5462222—
CatalystCopperHCID 23978—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
ProductHCID 23335287HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229448
Source datasetuspto-grants-1980_10
ORD IDord-7575242b326e478c8403a225747e6fa5
Source noteuspto-grants-1980_10