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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257457Generated: October 25, 2026

Diisopropylamine → 1-(2-Chlorophenyl)-3-(4-pyridyl)-butane

https://huagongshe.com/reaction/257457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant4-EthylpyridineHCID 10822—
Reactant1-(2-Bromoethyl)-2-chlorobenzeneHCID 2756963—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Chlorophenyl)-3-(4-pyridyl)-butaneHCID 1978332258.8%

Reaction Conditions

Temperature-50 °C

Reaction Steps

In a 200-ml flask, 0.94g (9.35 mmol) of diisopropyl amine and 15 ml of tetrahydrofuran were placed and cooled to -50° C. Then 6.5 ml (10.3 mmol) of n-butyl lithium (15% n-hexane solution) was added thereto under nitrogen atmosphere. The resulting mixture was stirred for 10 minutes, and a solution of 1.0 g (9.35 mmol) of 4-ethylpyridine dissolved in tetrahydrofuran was added dropwise. After stirring for 30 minutes at -50° C., the reaction temperature was gradually raised up to -10° C., which was kept for 30 minutes, and lowered again to -50° C. A solution of 2.05 g (9.35 mmol) of 2-chlorophenethyl bromide dissolved in tetrahydrofuran was added dropwise to the reaction mixture, and after stirring for 30 minutes at -50° C., the temperature was raised up to room temperature. Subsequently, water was added, tetrahydrofuran was distilled away under reduced pressure, and the residue was extracted with ethyl acetate. The extract was washed with saturated brine, then dried over anhydrous sodium sulfate. Then, the solvent was distilled away under reduced pressure, to obtain an oil. Said oil was purified by silica gel column chromatography, to obtain 1.35 g of the desired compound (yield: 58.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262420
Source datasetuspto-grants-1993_11
ORD IDord-780b878e9d6541c5b0b544cd0cfb5815
Source noteuspto-grants-1993_11