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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608186Generated: October 31, 2026

Sodium borohydride → HCID 19848717, compound

https://huagongshe.com/reaction/1608186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12281017HCID 12281017—
SolventEthanolHCID 702—
ProductHCID 19848717HCID 19848717—

Reaction Steps

A solution of ethyl 4-oxo-1-azabicyclo[3.3.1]non-3-yl carboxylate* (22 g, 0.104 moles) in ethanol (200 ml) was cooled in an ice bath to 5° C. and treated portionwise with sodium borohydride (4.0 g). The reaction was then allowed to warm to room temperature and stirred overnight. The solvent was then removed in vacuo, the residue partitioned between dichloromethane (200 ml) and water (75 ml) and the organic layer separated and dried (Na2SO4). Filtration and removal of the solvent afforded the required product as an oil (20.0 g), 85% pure by g.l.c. (OVl, 180° C.) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04870081
Source datasetuspto-grants-1989_09
ORD IDord-341f34e8947641668fb2998d4bdf62ad
Source noteuspto-grants-1989_09