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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276979Generated: October 31, 2026

2-Bromoethanol → 2-(3-nitrophenoxy)ethanol

https://huagongshe.com/reaction/2276979

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
Reactant3-NitrophenolHCID 11137—
ReactantSodium HydroxideHCID 14798—
SolventDimethylformamideHCID 6228—
Product2-(3-nitrophenoxy)ethanolHCID 4668927—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-nitrophenol (10 g, 71.9 mmol) in DMF (40 ml) was added NaOH pellets (3.16 g, 79.1 mmol) and 2-bromoethanol (5.6 ml, 79.1 mmol). The reaction mixture was heated at 60° C. for 18 h. LCMS indicated 65% conversion to the required product. The reaction mixture was diluted with water (10 ml) and was slowly neutralised with 2M HCl. The reaction mixture was extracted with EtOAc (50 ml) and washed with water (50 ml). The EtOAc layer dried (Na2SO4), filtered and evaporated to dryness. Flash column chromatography purification eluting with 30% EtOAc/heptane gave the required product (8.2 g, 62% yield). LCMS purity 100%, m/z 184 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133104B2
Source datasetuspto-grants-2015_09
ORD IDord-5cfbe114b68047aeb5deaf5662aec075
Source noteuspto-grants-2015_09