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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199402Generated: October 25, 2026

Sodium Bicarbonate → 3-Fluoro-4-(1-hydroxymethyl-propylamino)-benzonitrile

https://huagongshe.com/reaction/2199402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3,4-DifluorobenzonitrileHCID 587203—
Reactant2-Amino-1-butanol, (-)-HCID 2723856—
SolventDimethylformamideHCID 6228—
Product3-Fluoro-4-(1-hydroxymethyl-propylamino)-benzonitrileHCID 4365716133.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A 100 mL round bottom flask was charged with 3,4-difluorobenzonitrile (2.013 g, 14.5 mmol), sodium bicarbonate (1.59 g, 18.9 mmol), and L-(−)-2-amino-1-butanol (1.33 mL, 14.5 mmol). The contents were then dissolved in 40 mL N,N-dimethylformamide (anhydrous). The flask was heated to 90° C. and stirred overnight under N2. The reaction mixture was cooled to room temperature, poured onto water, and extracted with EtOAc (2 times). The organic layers were combined, washed with brine, dried (MgSO4), and concentrated. The resulting residue was purified via silica gel chromatography (gradient from 5% EtOAc/Hexanes to 10% EtOAc/Hexanes followed by 50% EtOAc/Hexanes) to afford 1.00 g (33% yield) of the title compound. 1H NMR (CDCl3, 500 MHz) δ: 7.28 (m, 1H), 7.21 (dd, J=11.3, 1.8 Hz, 1H), 6.72 (t, J=8.5 Hz, 1H), 4.49 (s, 1H), 3.77 (m, 1H), 3.68 (dt, J=10.0, 5.3 Hz, 1H), 3.48 (m, 1H), 1.87 (m, 1H), 1.72 (dqn, J=14.5, 7.5 Hz, 1H), 1.60 (dqn, J=14.5, 7.5 Hz, 1H), 1.00 (t, J=7.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359285B2
Source datasetuspto-grants-2016_06
ORD IDord-ac3c06ec996b46ceb368595d20da7475
Source noteuspto-grants-2016_06