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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773224Generated: November 2, 2026

Ethyl bromoacetate → Ethyl (2-formyl-4-methylphenoxy)acetate

https://huagongshe.com/reaction/1773224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzaldehyde, 2-hydroxy-5-methyl-HCID 69184—
SolventDimethylformamideHCID 6228—
ProductEthyl (2-formyl-4-methylphenoxy)acetateHCID 1315700576.6%

Reaction Steps

To a solution of 2-hydroxy-5-methylbenzaldehyde (2 g, 14.69 mmol) in 22 mL of DMF was added K2CO3 (4.06 g, 29.4 mmol) under N2 at room temperature. After the mixture was stirred for 10 min, ethyl 2-bromoacetate (1.625 mL, 14.69 mmol) was added. The reaction mixture was stirred at room temperature overnight, and filtered through Celite to remove solids. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel flash chromatography, 100% Heptane-20% Ethyl Acetate/80% Heptane, to give a white solid, ethyl 2-(2-formyl-4-methylphenoxy)acetate (2.5 g). LCMS retention time=1.19 minutes (LC method 3); MS (m+1)=222.9. 1H NMR (400 MHz, DMSO-d6) δ 1.20 (t, J=7.1 Hz, 3H), 2.28 (s, 3H), 4.17 (q, J=7.2 Hz, 2H), 4.95 (s, 2H), 7.08 (d, J=8.6 Hz, 1H), 7.45 (ddd, J=8.6, 2.5, 0.6 Hz, 1H), 7.51 (d, J=2.2 Hz, 1H), 10.41 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255093B2
Source datasetuspto-grants-2016_02
ORD IDord-daa75d7413cc444581635cac077a9887
Source noteuspto-grants-2016_02