Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880131Generated: November 1, 2026

Sodium borohydride → HCID 59326922, compound

https://huagongshe.com/reaction/1880131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 3-(2-fluoropyridin-3-yl)-4-nitrobutanoateHCID 59327206—
CatalystNickel DichlorideHCID 24385—
SolventEthanolHCID 702—
ProductHCID 59326922HCID 5932692223%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 3-(2-fluoropyridin-3-yl)-4-nitrobutanoate (0.991 g, 4.09 mmol) in EtOH (20 mL) at 0° C. was added nickel chloride (0.532 g, 4.10 mmol) and sodium borohydride (1.60 g, 42.3 mmol). The reaction mixture was stirred at 0° C. for 30 min, warmed to room temperature over 30 min, and stirred at room temperature for 30 min. The reaction mixture was quenched with saturated aqueous KH2PO4 and diluted with water and EtOAc. The mixture was filtered through a pad of Celite. The filtrate was extracted with EtOAc (6×) and the combined organic extracts were washed with brine (1×), dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography on silica gel (5% to 10% MeOH in DCM) gave 4-(2-fluoropyridin-3-yl)pyrrolidin-2-one (0.168 g, 0.932 mmol, 23% yield) as a colorless oil. MS (ESI, pos. ion) m/z: 181.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318718B2
Source datasetuspto-grants-2012_11
ORD IDord-e349523438214a46884ed76cb8496c0d
Source noteuspto-grants-2012_11