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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356223Generated: October 26, 2026

2-Bromoethanol → N-Ethyl-N-(beta-hydroxyethyl)-4-bromoaniline

https://huagongshe.com/reaction/356223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-bromo-N-ethylanilineHCID 11745656—
SolventWaterHCID 962—
ProductN-Ethyl-N-(beta-hydroxyethyl)-4-bromoanilineHCID 1894147369.5%

Reaction Conditions

Temperature125 °C

Reaction Steps

17.3 g (86.7 mmols) of N-ethyl-4-bromoaniline, 22.7 ml (1.5-fold equivalent weight) of N,N-diisopropylethylamine and 9.64 ml (1.5-fold equivalent weight) of 2-bromoethanol were mixed, and the mixture obtained was heated at 125° C. for 2 hours in an atmosphere of argon. Next, to the reaction solution obtained, 1.5 ml (0.1-fold equivalent weight) of diisopropylethylamine and 0.64 ml (0.1-fold equivalent weight) of 2-bromoethanol were added, and the mixture obtained was heated at 125° C. for 3 hours in an atmosphere of argon. Water was added to the reaction solution obtained, which was then extracted with ethyl acetate. The organic layer obtained was dried with anhydrous magnesium sulfate and then concentrated. The residue thus obtained was purified by silica gel column chromatography developing system (chloroform) to obtain 14.7 g of N-ethyl-N-(2-hydroxyethyl)-4-bromoaniline (yield: 69.5%; a colorless oily liquid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834575
Source datasetuspto-grants-1998_11
ORD IDord-007123975d5847128a691b561d3559d1
Source noteuspto-grants-1998_11