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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404310Generated: October 29, 2026

3-Bromo-4-(bromomethyl)benzonitrile → tert-butyl N-(2-bromo-4-cyanobenzyl)-N-methylglycinate

https://huagongshe.com/reaction/2404310

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-(bromomethyl)benzonitrileHCID 288436—
ReactantSarcosine t-butyl ester hydrochlorideHCID 11252350—
Producttert-butyl N-(2-bromo-4-cyanobenzyl)-N-methylglycinateHCID 66678124—

Reaction Steps

The title compound was prepared following the general procedure 10, starting from 2-bromo-4-cyanobenzyl bromide (Carbocor) and sarcosine tert-butyl ester hydrochloride. It was obtained as a white solid. 1H NMR (DMSO-d6, 300 MHz) δ 8.17 (d, J=1.6 Hz, 1H), 7.88 (dd, J=8.0, 1.6 Hz, 1H), 7.69 (d, J=8.0 Hz, 1H), 3.82 (s, 2H), 3.31 (s, 2H), 2.31 (s, 3H), 1.43 (s, 9H). LC/MS (Method B): 338.9, 340.9 (M+H)+. HPLC (Method A) Rt 3.10 min (Purity: 99.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802704B2
Source datasetuspto-grants-2014_08
ORD IDord-62a56fec43df4594bebd190f749ed425
Source noteuspto-grants-2014_08