Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740114Generated: November 4, 2026

Iodoethane → 4-(2-Ethoxy-naphthalen-1-ylmethyl)-1-[4(1-ethoxy-propyl)-2,6-dimethylphenyl]-3,5-diethyl-1H-pyrazole

https://huagongshe.com/reaction/1740114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantDichloromethaneHCID 6344—
ReactantSodium hydrideHCID 24758—
Reactant1-{4-[4-(2-Ethoxy-naphthalen-1-ylmethyl)-3,5-diethyl-pyrazol-1-yl]-3,5-dimethylphenyl}-propan-1-olHCID 21837329—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Ethoxy-naphthalen-1-ylmethyl)-1-[4(1-ethoxy-propyl)-2,6-dimethylphenyl]-3,5-diethyl-1H-pyrazoleHCID 21837342146.5%

Reaction Steps

Sodium hydride (60% mineral oil dispersion, 0.031 g, 0.78 mmol) was added portionwise to a solution of 1-{4-[4-(2-ethoxy-naphthalen-1-ylmethyl)-3,5-diethyl-pyrazol-1-yl]-3,5-dimethylphenyl}-propan-1-ol (0.123 g, 0.26 mmol) in 0.5 ml anhydrous tetrahydrofuran. After stirring 5 minutes, iodoethane (0.104 ml, 1.3 mmol) was added and the resulting mixture was stirred for 16 hours at ambient temperature. A second portion of sodium hydride (0.031 g of a 60% sodium hydride mineral oil dispersion; 0.78 mmol) was added, followed by a second portion of iodoethane (0.104 ml, 1.3 mmol). After stirring at ambient temperature for 4 hours, the reaction mixture was well-mixed with methylene chloride/aqueous sodium bicarbonate (10 ml of each). The aqueous phase was then twice extracted with 10 ml portions of fresh methylene chloride. The combined organic extracts were then dried over anhydrous sodium sulfate and concentrated in vacuo to afford a 190 mg residue. Flash chromatography of the entire sample (silica gel, 40 micron mesh; elution with ethyl acetate/hexanes=1:4 in volume) afforded the title compound (45 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968944
Source datasetuspto-grants-1999_10
ORD IDord-dd4bc209f2424709a4f985b907ea62f1
Source noteuspto-grants-1999_10