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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239135Generated: October 29, 2026

Sodium borohydride → HCID 86686043, compound

https://huagongshe.com/reaction/239135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86686044HCID 86686044—
SolventEthanolHCID 702—
ProductHCID 86686043HCID 8668604361.7%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642774B2
Source datasetuspto-grants-2014_02
ORD IDord-936df5545d174ddaa9cc044533dd8285
Source noteuspto-grants-2014_02