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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326517Generated: October 30, 2026

1-Iodohexane → HCID 23354763, compound

https://huagongshe.com/reaction/326517

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodohexaneHCID 12527—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 67686570HCID 67686570—
Solvent1-ButanolHCID 263—
ProductHCID 23354763HCID 2335476389.5%

Reaction Steps

In a 30 ml-round-bottomed flask, 1.07 g (3.01 mM) of 2-(4-hexylphenyl)-5-(3-fluoro-4-hydroxyphenyl)-5-(3-fluoro-4-hydroxyphenyl)thiazole prepared in Synthesis Example 7, 0.23 g (3.48 mM) of potassium hydroxide and 5 ml of butanol were placed and heated to provide a solution. To the solution, 0.74 g (3.49 mM) of hexyl iodide was gradually added under heat stirring, followed by stirring for 5 hours at about 90° C. After the reaction, the solvent in the reaction mixture was distilled off under reduced pressure and water was added to the residue to precipitate a crystal. The crystal was recovered by filtration and washed with water. The resultant crystal was purified by silica gel column chromatography (eluent: toluene) and recrystallized from a mixture solvent (toluene-methanol) to obtain 0.90 g of 2-(4-hexylphenyl)-5-(3-fluoro-4-hexyloxyphenyl)thiazole (Yield: 68.0%). ##STR51##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05269964
Source datasetuspto-grants-1993_12
ORD IDord-a0cc9a062d554ca79f1efe73970dc756
Source noteuspto-grants-1993_12