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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194385Generated: October 31, 2026

HCID 14520339, compound → HCID 178477816, compound

https://huagongshe.com/reaction/1194385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14520339HCID 14520339—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 178477816HCID 17847781683.9%

Reaction Steps

50.85 g (0.1 mole) of alpha-(6-chloro-4H-1,3-benzodioxin-8-yl)-1-triphenylmethyl-1H-imidazole-4-methanol (prepared in Example 1.C.1.), dissolved in 500 ml of acetic acid, are hydrogenolyzed in the presence of 3 g of 10% palladium on carbon for 2 hours at 80° C., under a hydrogen pressure of 2.41 bars. The catalyst is then filtered off and the solvent is distilled under reduced pressure. The residue obtained is extracted three times with diethyl ether to remove the triphenylmethane formed. It is subsequently recrystallized from 50 ml of acetonitrile. 21.2 g of 4-[(4H-1,3-benzodioxin-8-yl)methyl]-1H-imidazole hydrochloride are obtained. Yield: 83% of theory; M.P.: 168°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04814343
Source datasetuspto-grants-1989_03
ORD IDord-9e3cdc6883f5442790e551ffceef9bc5
Source noteuspto-grants-1989_03