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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572559Generated: October 26, 2026

4-(Bromomethyl)-3-fluorobenzonitrile → Tert-butyl 2-[(4-cyano-2-fluorobenzyl)amino]-2-methylpropanoate

https://huagongshe.com/reaction/572559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromomethyl)-3-fluorobenzonitrileHCID 2783149—
Reactanttert-Butyl 2-methylalaninateHCID 7019940—
ProductTert-butyl 2-[(4-cyano-2-fluorobenzyl)amino]-2-methylpropanoateHCID 66652709—

Reaction Steps

The title compound was prepared following general procedure 10 starting from tert-butyl 2-amino-2-methylpropanoate and 4-cyano-2-fluoro benzyl bromide. The title compound was isolated as colorless liquid. 1H NMR (DMSO-d6, 400 MHz) δ 7.78-7.75 (d, J=10.0 Hz, 1H), 7.71-7.65 (m, 2H), 3.70-3.68 (d, J=6.9 Hz, 2H), 2.55 (s, 1H), 1.44 (s, 9H), 1.19 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029405B2
Source datasetuspto-grants-2015_05
ORD IDord-080c1eee73904d978f295de8e8df4485
Source noteuspto-grants-2015_05