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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061639Generated: October 29, 2026

1,4-Dibromobutane → HCID 1204325, compound

https://huagongshe.com/reaction/2061639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantPhenylsulphonylacetonitrileHCID 82077—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
ProductHCID 1204325HCID 120432598%

Reaction Steps

629 mg (2.8 mmol) of benzyltriethylammonium chloride is added to 5 g (27.6 mmol) of benzenesulfonylacetonitrile and 6.55 g (30.3 mmol) of 1,4-dibromobutane in 50 ml of a 50% aqueous soda solution. The reaction mixture is stirred at room temperature for 3 h. It is then diluted with water and extracted with ethyl acetate. The organic phases are combined and washed with water. They are dried over magnesium sulfate, filtered and the solvents are evaporated. The residue is purified on silica gel (heptane/ethyl acetate, 50/50, v/v). 6.35 g of 1-benzenesulfonyl-cyclopentanecarbonitrile is obtained in the form of a beige powder. (Yield=98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283378B2
Source datasetuspto-grants-2012_10
ORD IDord-8099e96b5e5041d1b9ce1a57a76f51e5
Source noteuspto-grants-2012_10