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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720023Generated: October 31, 2026

Isopropanol → 1-(3-Chlorophenyl)cyclobutane-1-carbonitrile

https://huagongshe.com/reaction/720023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant1,3-DibromopropaneHCID 8001—
ReactantSodium hydrideHCID 24758—
Reactantm-ChlorophenylacetonitrileHCID 73722—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-(3-Chlorophenyl)cyclobutane-1-carbonitrileHCID 2190197971%

Reaction Steps

A solution of 3.37 g (22.2 mmol) of 3-Chlorobenzyl cyanide and 4.93 g (24.4 mmol) of 1,3-dibromopropane in 15 mL of ether was added dropwise into 1.17 g (48.8 mmol) of NaH in 60 mL of DMSO. The temperature was held between 25° and 35° by water bath cooling. The mixture was stirred at room temperature for 18 hours. The mixture was cooled in ice water and 3 mL of 2-propanol was added dropwise, followed by the addition of 50 mL of water. The mixture was extracted with hexane (3×100 mL), and the combined extracts were washed with water (3×75 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated to yield 3.0 g (71%) product as colorless oil. 1H NMR (CDCl3) δ 2.04–2.16 (m, 1H), 2.38–2.50 (m, 1H), 2.56–2.67 (m, 2H), 2.79–2.89 (m, 2H), 7.29–7.36 (m, 3H), 7.41–7.43 (m, 1H). 13C NMR (CDCl3) 17.3, 34.8, 40.1, 124.2, 126.2, 128.4, 130.5, 135.2, 142.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132551B2
Source datasetuspto-grants-2006_11
ORD IDord-b3da49642a4b42d7a4485fadcd6467ef
Source noteuspto-grants-2006_11