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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611760Generated: November 1, 2026

2-Chloroethanol → 2-(2-Nitrophenoxy)ethanol

https://huagongshe.com/reaction/611760

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantWaterHCID 962—
Reactant2-NitrophenolHCID 6947—
ReactantSodium HydroxideHCID 14798—
Solvent1-ButanolHCID 263—
Product2-(2-Nitrophenoxy)ethanolHCID 273705982%

Reaction Conditions

Temperature100 °C

Reaction Steps

10 g (71.88 mmol) 2-nitrophenol A1 and 3.59 g (89.86 mmol) sodium hydroxide were dissolved in 55 ml n-butanol and 5 ml water at 70° C., 6.26 ml (7.52 g, 93.44 mmol) 2-chloroethanol were slowly added drop by drop. This was followed by three days of vigorous stirring at 100° C. After cooling, the reaction mixture was filtrated, the precipitate washed with chloroform and the filtrate reduced. The residue was taken up in chloroform and washed three times with aqueous 10% sodium hydroxide solution. Then the organic phase was dried over sodium sulfate and was concentrated in vacuo. 10.8 g of bright yellow crystals were obtained; yield 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06001999
Source datasetuspto-grants-1999_12
ORD IDord-803d766689644a11b4247240b6f5a848
Source noteuspto-grants-1999_12