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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770157Generated: November 2, 2026

1-Iodohexane → HCID 20095029, compound

https://huagongshe.com/reaction/1770157

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodohexaneHCID 12527—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 20095042HCID 20095042—
Solvent1-ButanolHCID 263—
ProductHCID 20095029HCID 2009502976%

Reaction Steps

0.25 g (0.62 mM) of 2-octyl-5-[5-(4-hydroxyphenyl)pyrimidine-2-yl]indan, 0.07 g of 85% -potassium hydroxide, 0.2 ml of hexyl iodide and 5 ml of n-butanol were placed in a 20 ml-round bottomed flask, followed by heat-refluxing for 3.5 hours under stirring. After the reaction, the reaction mixture was poured into ice water. The resultant insoluble matter was recovered by filtration and dissolved in toluene, followed by washing with 3%-sodium thiosulfate aqueous solution. The water layer was subjected to extraction with toluene and the resultant toluene layer was added to the organic layer, followed by washing with saturated common salt aqueous solution, drying with anhydrous sodium sulfate and distilling-off of the solvent. The resultant crude product was purified by silica gel column chromatography (eluent: toluene) and recrystallized from a mixture solvent (toluene/methanol) to obtain 0.23 g of 2-octyl-5-[5-(4-hexyloxyphenyl)pyrimidine-2-yl]indan (Yield: 76.0%). ##STR139##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05385692
Source datasetuspto-grants-1995_01
ORD IDord-723122083b2c41f89fd41efcd67d90b4
Source noteuspto-grants-1995_01