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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194387Generated: November 1, 2026

Ammonia → HCID 178431335, compound

https://huagongshe.com/reaction/1194387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodiumHCID 5360545—
ReactantHCID 178431338HCID 178431338—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178431335HCID 17843133574.6%

Reaction Steps

94.13 g (0.317 mole) of alpha-(2,2-dimethyl-4H-1,3-benzodioxin-8-yl)-1H-imidazole-4-methanol hydrochloride (prepared in Example 3.1. or 3.5.) are introduced into 1 liter of anhydrous liquid ammonia. The solubilization of the reagent is completed by the addition of 1 liter of tetrahydrofuran. 14.6 g (0.634 mole) of sodium are then added piece by piece. 5 minutes after the sodium has disappeared, 34 g of ammonium chloride are added and the reaction mixture is stirred for 30 minutes. There is then added 1.56 liter of a 10% solution of methanol in toluene. The ammonia is then evaporated on a water-bath. 780 ml of water are then added and the organic phase is separated. The aqueous phase is extracted twice with 500 ml of toluene. The organic phases are combined and washed with 1 liter of water, then dried over anhydrous sodium sulfate and distilled under reduced pressure. The residue obtained is recrystallized from 900 ml of boiling acetone. There are thus obtained 57.8 g of 4-[(2,2-dimethyl-4H-1,3-benzodioxin-8-yl)methyl]-1H-imidazole; M.P.: 160°-170° C. Yield: 74.6% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04814343
Source datasetuspto-grants-1989_03
ORD IDord-31c00bc2485c4e72a073336af5f67a44
Source noteuspto-grants-1989_03