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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046775Generated: November 1, 2026

Sodium borohydride → 5,5-Dimethyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol

https://huagongshe.com/reaction/2046775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5,5-Dimethyl-3-(3-nitropyridin-4-yl)cyclohex-2-enoneHCID 59226475—
SolventMethanolHCID 887—
Product5,5-Dimethyl-3-(3-nitropyridin-4-yl)cyclohex-2-enolHCID 5922648974%

Reaction Steps

To a solution of 5,5-dimethyl-3-(3-nitropyridin-4-yl)cyclohex-2-enone (1.0 eq), and CeCl3-7H2O (1.2 eq) in MeOH (0.2 M) was added NaBH4 (1.0 eq) at 0° C. The solution was stirred for 1 hour, and then quenched by the addition of 5 mL of water. The volatiles were removed in vacuum and the residue was partitioned between EtOAc and H2O. The organic layer was separated and washed with brine. The combined aqueous was back extracted with EtOAc and the organic was washed with brine. The combined organics were dried over MgSO4, filtered and concentrated. The residue was purified by column (5% methanol in 1:1 ethyl acetate and hexanes) to give 5,5-dimethyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol (74%). LC/MS (m/z): MH+=249.2, Rt=0.76.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592455B2
Source datasetuspto-grants-2013_11
ORD IDord-4eea2b6f1ec544cdb604b86e42124885
Source noteuspto-grants-2013_11