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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099003Generated: October 30, 2026

Water → HCID 178444526, compound

https://huagongshe.com/reaction/2099003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 57793288HCID 57793288—
SolventDimethylformamideHCID 6228—
ProductHCID 178444526HCID 17844452689.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

4.0 g of the compound (b67) obtained in the second step was dissolved in 20 mL of N,N,-dimethylformamide. After suspending 2.5 g of potassium carbonate in the solution, 5.6 g of the compound (b68) was added thereto, followed by stirring for 6 hours at 70° C. After completing the reaction, water and toluene were added to the reaction mixture, followed by mixing. Thereafter, the mixture was left at rest to separate into an organic layer and an aqueous layer, followed by extracting to the organic layer. The resulting organic layer was washed sequentially with water, a 2N sodium hydroxide aqueous solution, a saturated sodium chloride aqueous solution and water, and then concentrated under reduced pressure to obtain a residue. 7.7 g of the residue was purified by a preparative column chromatography using a mixed solvent of heptane and toluene (heptane/toluene=3/1 by volume) as a developing solvent and silica gel as a mediator, and further purified by repeating recrystallization from a mixed solvent of heptane and Solmix A-11 (heptane/Solmix A-11=2/1 by volume) to obtain 3-chloro-2-fluoro-4-(trans-4-pentyl-cyclohexylmethoxy)-4′-propylbiphenyl (C264) as colorless crystals. The yield was 89.5% based on the compound (b67).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569258B2
Source datasetuspto-grants-2009_08
ORD IDord-4e71eed955f54c15ba4320e5dace38ea
Source noteuspto-grants-2009_08