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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004535Generated: October 30, 2026

Pyridine → HCID 178447886, compound

https://huagongshe.com/reaction/1004535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTolueneHCID 1140—
Reactant3-Fluoro-4-(trifluoromethoxy)phenolHCID 2783357—
ReactantHCID 178447883HCID 178447883—
SolventWaterHCID 962—
ProductHCID 178447886HCID 17844788694.2%

Reaction Steps

Then, 1.3 g (6.5 mmol) of 3-fluoro-4-trifluoromethoxyphenol, 0.8 ml of pyridine, and 3 ml of toluene were mixed. To this mixture was added dropwise 3 ml of toluene solution containing 6.5 mmol of 4-(trans-4-propylcyclohexyl)benzoyl chloride at room temperature in 5 minutes. After the dropping was finished, they were reacted at 50° C. for 3 hours. After finishing of the reaction, 15 ml of water was added to the reaction product, and then extracted with 40 ml of toluene. The organic layer thus obtained was washed with 6N-hydrochloric acid thrice, 2N-sodium hydroxide thrice, and water thrice, and then dried over anhydrous magnesium sulfate. Solvent was distilled off at a reduced pressure and the residue was subjected to a silica gel column chromatography (eluent: toluene) to obtain 2.6 g of a crude 3-fluoro-4-trifluoromethoxyphenyl 4-(trans-4-propyl-cyclohexyl)benzoate. This product was recrystallized from a mixed solvent of heptane/ether (1/1) to obtain 2.4 g (yield: 85.6%) of the subject compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051288
Source datasetuspto-grants-2000_04
ORD IDord-79dc29aea7da4e6bac2f508dd3df9ab8
Source noteuspto-grants-2000_04