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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868431Generated: October 31, 2026

Sodium borohydride → HCID 21288484, compound

https://huagongshe.com/reaction/868431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13560734HCID 13560734—
SolventEthanolHCID 702—
ProductHCID 21288484HCID 21288484—

Reaction Steps

The ketone, trans-3-hexanoyl stilbene of Example 20 (1 g) was dissolved in ethanol, and sodium borohydride (0.2 g) was added. The mixture was stirred overnight. Excess of the borohydride was destroyed by carefully adding a dilute HCl solution. The aqueous solution was extracted thoroughly with ether, and then the ether extract was washed with brine and dried. On removal of all volatiles, the pure alcohol was obtained as a clear, colorless liquid in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04778931
Source datasetuspto-grants-1988_10
ORD IDord-30b76913f71145c78c8cc230ceca733d
Source noteuspto-grants-1988_10