Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517731Generated: November 1, 2026

Thionyl Chloride → 5-(Chloromethyl)-1-[4-(pentafluoro-lambda6-sulfanyl)phenyl]-1H-tetrazole

https://huagongshe.com/reaction/517731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant{1-[4-(Pentafluoro-lambda6-sulfanyl)phenyl]-1H-tetrazol-5-yl}methanolHCID 86691877—
SolventTolueneHCID 1140—
Product5-(Chloromethyl)-1-[4-(pentafluoro-lambda6-sulfanyl)phenyl]-1H-tetrazoleHCID 86691879—

Reaction Steps

Thionyl chloride (1.72 g, 14.4 mmol) was added to a stirred solution of {1-[4-(pentafluoro-λ6-sulfanyl)phenyl]-1H-tetrazol-5-yl}methanol (Intermediate 44, 3.50 g, 11.6 mmol) in toluene (40 mL), SOCl2 at room temperature. The reaction mixture was stirred for 4 hr at reflux. The reaction mixture was concentrated under vacuum. The residue was diluted with DCM and washed with ice-water, saturated aq NaHCO3 and brine solution, dried over anhydrous Na2SO4, and concentrated under reduced pressure to give the crude compound. This was purified by column chromatography (100-200 mesh silica gel), eluted with 20%-30% EtOAc/pet-ether to give the title compound as a brown gum (3.50 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115132B2
Source datasetuspto-grants-2015_08
ORD IDord-f7aa9686189d4119b57558a68359dcb3
Source noteuspto-grants-2015_08