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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzaldehyde, 2-hydroxy-5-methyl- | HCID 69184 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl (2-formyl-4-methylphenoxy)acetate | HCID 13157005 | 76.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255093B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-daa75d7413cc444581635cac077a9887 |
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| Source note | uspto-grants-2016_02 |
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