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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367979Generated: October 30, 2026

Ethyl Bromide → 3-Ethoxy-6-fluoro-2-hydroxy-benzaldehyde

https://huagongshe.com/reaction/2367979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
Reactant6-Fluoro-2,3-dihydroxybenzaldehydeHCID 86664732—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product3-Ethoxy-6-fluoro-2-hydroxy-benzaldehydeHCID 8666473489.1%

Reaction Steps

To a solution of 6-fluoro-2,3-dihydroxy-benzaldehyde (1.00 g, 6.40 mmol) in dry DMSO (10 mL) was added NaOBut (1.23 g, 12.81 mmol) and ethyl bromide (0.77 g, 7.04 mmol) under N2 and stirred at RT for 18 h. The resultant mixture was diluted with water, acidified to pH ˜6 with 2N.HCl and extracted with EtOAc (4×25 mL). Combined organic layers were washed with water and brine and dried over MgSO4. Filtration and removal of the solvent under reduced pressure provided 1.05 g (5.70 mmol, 89%) of the title compound as yellow solid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 10.24 (s, 1H), 7.04 (dd, J=8.8, 5.3 Hz, 1H), 6.61-6.50 (m, 1H), 4.09 (q, J=7.0 Hz, 3H), 1.46 (t, J=7.0 Hz, 3H); 19F NMR (376 MHz, CHLOROFORM-d) δ ppm −132.19-−132.15 (m, 1F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703742B2
Source datasetuspto-grants-2014_04
ORD IDord-7aefcc4fed0e411585ccf84af0939f53
Source noteuspto-grants-2014_04