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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101207Generated: October 31, 2026

4-Bromobenzyl bromide → HCID 61517831, compound

https://huagongshe.com/reaction/2101207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant(2-ETHOXY-ETHYL)-ETHYL-AMINEHCID 520890—
SolventDimethylformamideHCID 6228—
ProductHCID 61517831HCID 6151783197.3%

Reaction Steps

4-Bromobenzylbromide (4.01 g) was added to a solution of N-(2-ethoxyethyl)ethanamine (3.64 g) in DMF (40 ml). After stirring at ambient temperature for 18 h, the mixture was partitioned between diethyl ether and water. The organic phase was extracted with 2N aqueous hydrochloric acid which was then taken to pH 10 by addition of 2N sodium hydroxide solution. This was then extracted with diethyl ether which was dried and the solvent removed under vacuum to yield the title compound as a yellow oil (4.25 g). 1H NMR (DMSO-D6) 0.95 (t, 2H), 2.45 (q, 3H), 2.55 (t, 2H), 3.2 (s, 3H), 3.36 (t, 2H), 3.52 (s, 2H), 7.24 (d, 2H), 7.46 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572826B2
Source datasetuspto-grants-2009_08
ORD IDord-f947c46f00b34de28672a048ca3072cc
Source noteuspto-grants-2009_08