HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239135Generated: October 29, 2026
Sodium borohydride → HCID 86686043, compound
https://huagongshe.com/reaction/239135
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86686044 | HCID 86686044 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86686043 | HCID 86686043 | 61.7% |
Reaction Steps
21.6 g sodium borohydride was added to 130 g 1-benzyl-4-(5-methyl-oxazol-2-yl)-pyridinium in 1.5 L ethanol at 0° C. under nitrogen. The reaction was stirred 30 min at 0° C. and 2 h at RT. The mixture was concentrated and treated with water and ethyl acetate. The organic layer was separated and washed with brine and evaporated. The residue was purified by chromatographie on silica to give 81.2 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642774B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-936df5545d174ddaa9cc044533dd8285 |
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| Source note | uspto-grants-2014_02 |
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