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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360634Generated: November 2, 2026

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

https://huagongshe.com/reaction/2360634

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 numberUS08686032B2
Source datasetuspto-grants-2014_04
ORD IDord-e78ca8af3b8e433997472bd0fdbe9ac0
Source noteuspto-grants-2014_04