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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657462Generated: November 1, 2026

Sodium borohydride → HCID 21450364, compound

https://huagongshe.com/reaction/1657462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 131710266HCID 131710266—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 21450364HCID 21450364—

Reaction Steps

This pyridinium bromide (5.86g.) was dissolved in a mixture of ethanol (70 ml.) and water (23 ml.) and sodium borohydride (0.74g.) was added portionwise to the stirred solution at ambient temperature. At the end of the addition, the solution was stirred for a further 0.5 hours and was then diluted with diethyl ether (300 ml.) and water (300 ml.). The organic layer was separated, dried over anhydrous potassium carbonate and evaporated under reduced pressure. The residual amber gum (4.96g.) was purified via column chromatography on silica gel using 60°-80° petroleum ether/ethyl acetate mixtures as eluent to give 2,2-Dimethyl-5-methoxy-4-[1-(2-naphthylmethyl)-1,2,5,6-tetrahydropyrid-4-yl]-7-n-pentylchroman as an orange oil (2.70g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03960880
Source datasetuspto-grants-1976_06
ORD IDord-6086300b163c4aa89146be4e0c7421a5
Source noteuspto-grants-1976_06