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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727855Generated: November 1, 2026

Thionyl Chloride → HCID 19825181, compound

https://huagongshe.com/reaction/727855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 18417756HCID 18417756—
SolventTolueneHCID 1140—
ProductHCID 19825181HCID 19825181—

Reaction Steps

4.0 g (17.5 mmol) of 1-(3-bromophenyl)-butanol is stirred with 4 ml of thionyl chloride for 1 hour at room temperature. 10 ml of toluene is added to the reaction mixture. 1-Chloro-1-(3-bromophenyl)-butanol is obtained after concentration by evaporation in a vacuum. 1.3 g of imidazole is dissolved in 20 ml of dimethylformamide and mixed with 0.6 g of sodium hydride (80% in oil) under argon protective gas atmosphere. It is stirred for 1 hour at room temperature. The chlorine compound is instilled into 15 ml of dimethylformamide and allowed to stand overnight. The mixture is precipitated in 200 ml of water and extracted with ethyl acetate. The organic phase is concentrated by evaporation in a vacuum and then distilled on a bulb tube at 150° C./0.03 mbar. 1.6 g of 1-[1-(3-bromophenyl)-butyl]-imidazole is obtained as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045558
Source datasetuspto-grants-1991_09
ORD IDord-5df55939a11e4d03bdbe26c1f91a06cd
Source noteuspto-grants-1991_09