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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166152Generated: October 31, 2026

4-Nitrophenethyl alcohol → 1-[2-[(6-Bromohexyl)oxy]ethyl]-4-nitrobenzene

https://huagongshe.com/reaction/2166152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenethyl alcoholHCID 7494—
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
Product1-[2-[(6-Bromohexyl)oxy]ethyl]-4-nitrobenzeneHCID 135927841,851.4%

Reaction Steps

4-Nitrobenzeneethanol (10.25 g), 1,6-dibromohexane (27 ml) tetra-n-butylammonium bisulphate (1.7 g) and 12.5M aqueous sodium hydroxide (55 ml) were stirred together for 40 h. The mixture was diluted with water (250 ml), extracted with ER (3×350 ml) and the combined extracts were washed consecutively with water (250 ml) and brine (250 ml), dried and evaporated to give an oil (42.6 g). The oil was purified by FCC eluting with ER-CX (0:100→1:19) to give the title compound as a yellow oil (9.52 g). T.l.c. (ER-CX 1:19) Rf 0.11. The following compounds were similarly prepared:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943591
Source datasetuspto-grants-1990_07
ORD IDord-516dee78724c40dbb49cbca4a092ea52
Source noteuspto-grants-1990_07