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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091105Generated: October 25, 2026

Sodium Iodide → Noradenalone hydrochloride

https://huagongshe.com/reaction/1091105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium AzideHCID 33557—
Reactant2-Chloro-3',4'-dihydroxyacetophenoneHCID 66834—
SolventAcetoneHCID 180—
ProductNoradenalone hydrochlorideHCID 19983150.4%

Reaction Conditions

Temperature40 °C

Reaction Steps

10 g (53.6 mmol) of 2-chloro-3',4'-dihydroxyacetophenone was dissolved in 50 ml of acetone, and 600 mg (4.0 mmol) of sodium iodide and 5.23 g (80.5 mmol) of sodium azide were added thereto. The mixture was refluxed for 24 hours. The insolubles in the reaction solution were removed by filtration, and the filtrate was concentrated under reduced pressure. To the reaction solution, ethyl acetate was added, and the mixture was washed sequentially with water and with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the oily residue was dissolved in 100 ml of methanol and 13.6 ml of concentrated hydrochloric acid. 1.5 g of 10% palladium carbon catalyst was added to the solution, and the mixture was stirred under heating at 40° C. under a hydrogen gas stream for 5 hours. The reaction solution was filtered, and the filtrate was concentrated under reduced pressure. To the concentrated residue, actone was added, and the precipitated crystals were collected by filtration to obtain 5.5 g (yield: 50.4%) of 2-amino-3',4'-dihydroxyacetophenone hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05084453
Source datasetuspto-grants-1992_01
ORD IDord-5de5646c18d64af099c28f4a5094a92f
Source noteuspto-grants-1992_01