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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878428Generated: October 26, 2026

Hydrochloric Acid → 2-Chloro-5-phenyl-1,3,4-thiadiazole

https://huagongshe.com/reaction/878428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Amino-5-phenyl-1,3,4-thiadiazoleHCID 219408—
ReactantSodium NitriteHCID 23668193—
CatalystCopperHCID 23978—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Chloro-5-phenyl-1,3,4-thiadiazoleHCID 253145—

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred suspension of 2-amino-5-phenyl-[1,3,4]thiadiazole (6.45 g, 36.4 mmol; Aldrich) and copper (230 mg, 3.6 mmol; Aldrich) in hydrochloric acid (36 mL, 12 M) and glacial acetic acid (180 mL) was chilled to 0° C. and treated with a solution of sodium nitrite (2.64 g, 38.2 mmol; Aldrich) in water (12 mL), added dropwise over 40 minutes. After stirring at room temperature for 4 hours, the mixture was poured into ice water. The aqueous solution was extracted with chloroform (3×), and the combined extracts were washed sequentially with 5% sodium bicarbonate and brine, and dried over sodium sulfate. The crude product was filtered through a short silica gel plug with chloroform to afford the title product: 1H NMR (300 MHz, CDCl3) δ ppm 7.46-7.55 (m, 3H), 7.85-7.93 (m, 2H). MS (DCI/NH3) m/e 197/199 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987453B2
Source datasetuspto-grants-2015_03
ORD IDord-8e4a22c8b17949d694bd4c6123376d79
Source noteuspto-grants-2015_03