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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73569Generated: October 29, 2026

Sodium borohydride → HCID 59226486, compound

https://huagongshe.com/reaction/73569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(3-Nitropyridin-4-yl)cyclohex-2-enoneHCID 59226544—
SolventEthanolHCID 702—
ProductHCID 59226486HCID 5922648699%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-(3-nitropyridin-4-yl)cyclohex-2-enone (1.0 equiv.) was added EtOH (1.1M) and CeCl3-7H2O (1.3 equiv.). The reaction was cooled to 0° C., then NaBH4 (1.3 equiv.) was added in portions. Stirred for 2 h at 0° C., then quenched by adding water, concentrated to remove the EtOH, added EtOAc, extracted the organics, dried with brine, then Na2SO4, and concentrated to yield 3-(3-nitropyridin-4-yl)cyclohex-2-enol (99%). LC/MS=221.1 (M+H), LC=2.24 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829193B2
Source datasetuspto-grants-2014_09
ORD IDord-5d3ce4be06fd43e188e2e5f5a11ea8fc
Source noteuspto-grants-2014_09