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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216332Generated: October 25, 2026

4-(1,2,3-Thiadiazol-4-yl)benzaldehyde → 1-[4-(1,2,3-Thiadiazol-4-yl)phenyl]ethanol

https://huagongshe.com/reaction/216332

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1,2,3-Thiadiazol-4-yl)benzaldehydeHCID 2776453—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product1-[4-(1,2,3-Thiadiazol-4-yl)phenyl]ethanolHCID 68667674—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Methylmagnesium chloride (3 M in tetrahydrofuran) (0.83 mL, 2.5 mmol) was added to a −78° C. solution of 4-(1,2,3-thiadiazol-4-yl)benzaldehyde (473 mg, 2.5 mmol) in tetrahydrofuran (10 mL). After stirring at −78° C. for 2 h, the reaction mixture was quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried (magnesium sulfate) and concentrated in vacuo. Chromatography over silica eluting with 0-100% ethyl acetate/hexane afforded 1-[4-(1,2,3-thiadiazol-4-yl)phenyl]ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193228B2
Source datasetuspto-grants-2012_06
ORD IDord-9a84652538d347e2ac624294d371ab00
Source noteuspto-grants-2012_06