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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219878Generated: October 30, 2026

Potassium Carbonate → tert-butyl N-(5-cyano-2-fluorobenzyl)-N-methylglycinate

https://huagongshe.com/reaction/219878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSarcosine t-butyl ester hydrochlorideHCID 11252350—
Reactant3-(Bromomethyl)-4-fluorobenzonitrileHCID 16227236—
SolventAcetonitrileHCID 6342—
Producttert-butyl N-(5-cyano-2-fluorobenzyl)-N-methylglycinateHCID 67529926—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5-cyano-2-fluorobenzylbromide (CARBOCORE; CO-0137; 1.50 g; 7.01 mmol; 1 eq.), sarcosine tert-butyl ester hydrochloride (BACHEM; F-1135; 1 527.73 mg; 8.41 mmol; 1.20 eq.) and potassium carbonate (2.91 g; 21.02 mmol; 3 eq.) in CH3CN (25 mL) was stirred at 60° C. for 6 hours then at RT for one night. The acetonitrile was evaporated in vacuo and the resulting mixture diluted with water. Extraction with EtOAc, washing with NaCl sat. solution, drying over magnesium sulfate and concentration in vacuo gave the title compound as a slightly yellow oil (1.9 g; 97%). 1H NMR (CDCl3) δ 7.86 (dd, J=6.5, 2.0 Hz, 1H), 7.59-7.53 (m, 1H), 7.13 (t, J=9.0 Hz, 1H), 3.78 (s, 2H), 3.23 (s, 2H), 2.38 (s, 3H), 1.49 (s, 9H). 19F NMR (CDCl3) δ-108.3. GC/MS: 278. LC/MS (Method B): 279.1 (M+H)+. HPLC (Method A) Rt 2.25 min (Purity: 91.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-aa8828141f2547d6805209557794760e
Source noteuspto-grants-2012_06