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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004776Generated: October 25, 2026

6-Bromo-1-hexanol → N-ethyl-N-(6-hydroxyhexyl)-4-bromoaniline

https://huagongshe.com/reaction/1004776

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-1-hexanolHCID 77970—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-bromo-N-ethylanilineHCID 11745656—
SolventWaterHCID 962—
ProductN-ethyl-N-(6-hydroxyhexyl)-4-bromoanilineHCID 18793525100%

Reaction Conditions

Temperature110 °C

Reaction Steps

36.8 g (184.1 mmols) of N-ethyl-4-bromoaniline, 48.1 ml (1.5-fold equivalent weight) of N,N-diisopropylethylamine and 28.9 ml (1.2 equivalent) of 6-bromohexanol were mixed, and the mixture obtained was heated at 110° C. for 14 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 heated under reduced pressure (160° C./0.3 torr), and the components distilled out were removed to obtain 55.6 g of crude N-ethyl-N-(6-hydroxyhexyl)-4-bromoaniline (yield: 100%; a dark-brown oily liquid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051722
Source datasetuspto-grants-2000_04
ORD IDord-43f38d4b835a4852888afb02c2db9b16
Source noteuspto-grants-2000_04