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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404308Generated: October 31, 2026

Potassium Carbonate → tert-butyl N-(4-cyano-2-fluorobenzyl)-N-methylglycinate

https://huagongshe.com/reaction/2404308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Bromomethyl)-3-fluorobenzonitrileHCID 2783149—
ReactantSarcosine t-butyl ester hydrochlorideHCID 11252350—
SolventAcetoneHCID 180—
Producttert-butyl N-(4-cyano-2-fluorobenzyl)-N-methylglycinateHCID 6667767899.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 4-cyano-2-fluorobenzyl bromide (250 g, 1.17 mol), sarcosine tert-butyl ester hydrochloride (212.2 g, 1.17 mol) and potassium carbonate (484 g, 3.50 mol) in acetone (2 L) was stirred 24 hours at 50° C. and 18 hours at RT. The reaction mixture was filtered and the filtrate was concentrated under vacuum. The residue was taken up with water (1 L) and extracted with ethyl acetate (2×1 L). The combined organic layers were washed with water (1 L), dried (MgSO4) and concentrated under vacuum to give the title compound as a yellow-brown oil (325 g, quantitative). 1H NMR (DMSO-d6, 300 MHz) δ 7.82 (dd, J=9.9, 1.4 Hz, 1H), 7.70 (dd, J=7.9, 1.5 Hz, 1H), 7.64 (m, 1H), 3.78 (s, 2H), 3.23 (s, 2H), 2.27 (s, 3H), 1.42 (s, 9H). LC/MS (Method B): 279.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802704B2
Source datasetuspto-grants-2014_08
ORD IDord-9da44555de3143b2883cd780d65e232c
Source noteuspto-grants-2014_08