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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877956Generated: November 2, 2026

Thionyl Chloride → 1-(2-Bromobenzyl)-5-(3-chloropropyl)-1H-imidazole

https://huagongshe.com/reaction/1877956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-[3-(2-Bromobenzyl)-3H-imidazole-4-yl]propan-1-olHCID 58827179—
SolventDichloromethaneHCID 6344—
Product1-(2-Bromobenzyl)-5-(3-chloropropyl)-1H-imidazoleHCID 58827085—

Reaction Steps

To a solution of SOCl2 (0.55 mL, 7.54 mmol) in CH2Cl2 (15 mL) at 0° C. is added 3-[3-(2-bromobenzyl)-3H-imidazol-4-yl]propan-1-ol in portion and the resulting white suspension is refluxed for 1.5 h. The mixture is cooled with ice and collected to give a buff-colored solid, which is partitioned between CH2Cl2 and saturated aqueous NaHCO3. The organic layer is washed with brine, dried over anhydrous Na2SO4, and concentrated to give an oil. MS (ESI) m/z 313 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314097B2
Source datasetuspto-grants-2012_11
ORD IDord-08e16eeb61144593bf58b95b3ab526fc
Source noteuspto-grants-2012_11