HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244657Generated: October 31, 2026
Ammonium Chloride → HCID 178466117, compound
https://huagongshe.com/reaction/2244657
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59214390 | HCID 59214390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178466117 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678820B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-43777681fc2849259335494510bb2192 |
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| Source note | uspto-grants-2010_03 |
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