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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734786Generated: October 27, 2026

Dimethylformamide → 2-(4-Iodo-2-methyl-phenoxy)-ethanol

https://huagongshe.com/reaction/734786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-BromoethanolHCID 10898—
ReactantSodium hydrideHCID 24758—
Reactant4-Iodo-2-methylphenolHCID 143713—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Iodo-2-methyl-phenoxy)-ethanolHCID 4055115—

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere, 2.34 g (10 mmol) of 4-iodo-2-methylphenol was added batchwise to a suspension of 0.48 g (11 mmol) of NaH in 50 mL of THF cooled to 0° C. and the mixture was stirred for a further 30 minutes at this temperature. Then 0.85 mL (12 mmol) of 2-bromoethanol dissolved in 5 mL of THF was added dropwise and the mixture was stirred for 18 hours at RT. 5 mL of DMF was added and the reaction mixture was heated to 70° C. for 8 hours. It was evaporated down in vacuo, the residue was taken up in water, extracted exhaustively with EtOAc and dried over sodium sulfate. After the desiccant and solvent had been eliminated, the residue was purified by chromatography on silica gel (cyc/EtOAc 7:3). Yield: 0.39 g (14% of theoretical); C9H11IO2 (M=278.091); calc.: molpeak (M+H)+: 279; found: molpeak (M+H)+: 279; Rf value: 0.28 (silica gel, cyc/EtOAc 2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592358B2
Source datasetuspto-grants-2009_09
ORD IDord-d2247dbd4c25454d95dfebd20348a6a9
Source noteuspto-grants-2009_09