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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219885Generated: October 26, 2026

Potassium Carbonate → tert-butyl N-(5-cyano-2-fluorobenzyl)-N-methyl-beta-alaninate

https://huagongshe.com/reaction/219885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 3-(methylamino)propanoateHCID 14760311—
Reactant3-(Bromomethyl)-4-fluorobenzonitrileHCID 16227236—
SolventAcetonitrileHCID 6342—
Producttert-butyl N-(5-cyano-2-fluorobenzyl)-N-methyl-beta-alaninateHCID 66677998—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5-cyano-2-fluorobenzylbromide (CARBOCORE; CO-0137; 1.50 g; 7.01 mmol; 1 eq.), tert-butyl N-methyl-beta-alaninate (1.34 g; 8.41 mmol; 1.20 eq.) (prepared as described by Howard N., I. et al. in Bioorg. Med. Chem. 11 (2003), 3083-3099) and potassium carbonate (1.94 g; 14.02 mmol; 2 eq.) in CH3CN (25 mL) was stirred at 60° C. for 6 hours then at RT for 16 hours. The acetonitrile was evaporated in vacuo and the resulting mixture diluted with water. Extraction with EtOAc, washing with NaCl sat. solution, drying over sodium sulfate and concentration in vacuo gave title compound as a slightly yellow oil (1.9 g; 92%). 1H NMR (CDCl3) δ 7.79 (dd, J=6.7, 2.1 Hz, 1H), 7.57-7.52 (m, 1H), 7.11 (t, J=8.9 Hz, 1H), 3.57 (s, 2H), 2.74 (t, J=7.1 Hz, 2H), 2.43 (t, J=7.1 Hz, 2H), 2.22 (s, 3H), 1.45 (s, 9H). LC/MS (Method B): 293.2 (M+H)+. HPLC (Method A) Rt 2.44 min (Purity: 86.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-c8ca3a328c884567a1cdf62584df45a8
Source noteuspto-grants-2012_06