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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552867Generated: October 30, 2026

Ammonium Chloride → HCID 178466117, compound

https://huagongshe.com/reaction/552867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59214390HCID 59214390—
SolventEthanolHCID 702—
ProductHCID 178466117HCID 178466117—

Reaction Steps

To a solution of 5-[3-(1H-benzimidazol-6-yl)-1,2,4-oxadiazol-5-yl]-2-(2,2,2-trifluoro-1-methylethoxy)benzaldehyde (80 mg) in ethanol (3 ml) was added NaBH4 (9 mg) at 0° C. After stirring at room temperature for 0.5 hour, a saturated NH4Cl solution (10 ml) was added thereto, followed by extraction with EtOAc (20 ml). The organic layer was washed with saturated brine, dried over anhydrous MgSO4, and then filtered, and the filtrate was concentrated. To a solution of the residue (78 mg) in dioxane was added a 4M HCl/dioxane solution, followed by concentration. The resulting powder was recrystallized with IPA (10 ml) to obtain [5-[3-(1H-benzimidazol-5-yl)-1,2,4-oxadiazol-5-yl]-2-(2,2,2-trifluoro-1-methylethoxy)phenyl]methanol hydrochloride (70 mg) as white powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951825B2
Source datasetuspto-grants-2011_05
ORD IDord-1bea74f7d2e545368052838533a1709c
Source noteuspto-grants-2011_05