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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604470Generated: October 30, 2026

Hydrochloric Acid → HCID 57709598, compound

https://huagongshe.com/reaction/604470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
ReactantThioureaHCID 2723790—
ReactantHCID 10487846HCID 10487846—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 57709598HCID 57709598—

Reaction Steps

1-Phenyl-2-(2H-tetrazol-5-yl)-ethanone (3.3 g, 17.5 mmol), ethyl iodide (1.4 g, 17.5 mmol) and potassium carbonate (2.4 g, 17.5 mmol) was heated at reflux in acetone (50 mL) for 5 h under argon. The reaction mixture was then poured into water, made acidic with 6M HCl and extracted with diethyl ether. The organic extract was dried and evaporated to a red/orange oil. The oil was dissolved in diethyl ether (100 mL) and bromine (17.5 mmol) was added. The mixture was stirred over night at ambient temperature, then the solvent was removed in vacuo and the residue was redissolved in ethanol (100 mL). Thiourea (35 mmol) was added, and the resulting mixture was heated at reflux for 10 min., after which a solid precipitated. The reaction mixture was poured into water containing NaOH (17.5 mmol), and the orange crude product was recovered by filtration. The crude product was recrystallized from acetonitrile to give pale yellow solid. Yield: 0.6 g, 17%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910613B2
Source datasetuspto-grants-2011_03
ORD IDord-3cc470bf08de49578e814dc0c3afa2c6
Source noteuspto-grants-2011_03