Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990851Generated: October 25, 2026

Iodoethane → 3-Ethoxy-5-(hydroxymethyl)phenol

https://huagongshe.com/reaction/1990851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Dihydroxybenzyl alcoholHCID 34661—
SolventDimethylformamideHCID 6228—
Product3-Ethoxy-5-(hydroxymethyl)phenolHCID 5902968242%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-hydroxymethyl-benzene-1,3-diol (0.5 g, 3.57 mmol, 1.0 equiv) in DMF (5 mL) was added K2CO3 (0.99 g, 7.14 mmol, 2.0 equiv) and ethyl iodide (0.29 mL, 0.43 g, 3.93 mmol, 1.1 equiv) and the reaction mixture stirred under Ar at 60° C. for 4 h. The K2CO3 was removed by filtration, the filtrate extracted with ethyl acetate (3×50 mL), the combined organic phases washed with a sat. solution of sodium chloride (1×50 ml) and dried over Na2SO4. The solvent was removed by evaporation under reduced pressure and the crude material purified with column chromatography on silica eluting with a gradient of hexane/ethyl acetate (4:1→2:1) providing 0.25 g (42%) of the title compound. 1H NMR (250 MHz, CDCl3): δ 1.40 (t, J=7.0 Hz, 3H), 4.02 (q, J=7.0 Hz, 2H), 4.61 (d, J=5.6 Hz, 2H), 4.91 (br s, 1H), 6.29-6.31 (m, 1H), 6.43 (br s, 1H), 6.49 (br s, 1H). MS (EI): 168.0 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645753B2
Source datasetuspto-grants-2010_01
ORD IDord-e9b05f10b5874f5ca7fb77473efb4736
Source noteuspto-grants-2010_01