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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517744Generated: October 31, 2026

Thionyl Chloride → HCID 68074343, compound

https://huagongshe.com/reaction/517744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 66654834HCID 66654834—
SolventTolueneHCID 1140—
ProductHCID 68074343HCID 6807434327.8%

Reaction Steps

Thionyl chloride (0.22 g, 1.85 mmol) was added at room temperature to a solution of {1-[5-(Trifluoromethyl)-2-pyridinyl]-1H-tetrazol-5-yl}methanol (Intermediate 58, 0.20 g, 0.82 mmol) in toluene, and the reaction mixture was stirred for 2 hr at reflux. The reaction mixture was concentrated under vacuum. The residue was diluted with DCM and washed with ice-water, saturated NaHCO3 and brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure to afford the crude product. This was purified by column chromatography (60-120 mesh silica gel) eluting with 0-20% ethyl acetate/pet ether to give the title compound (60 mg) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115132B2
Source datasetuspto-grants-2015_08
ORD IDord-31801dc0f202486589ae39f2bb171548
Source noteuspto-grants-2015_08