HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625580Generated: October 26, 2026
Methyl 4-chloro-2-methoxybenzoate → Methyl 4-ethyl-2-methoxybenzoate
https://huagongshe.com/reaction/1625580
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-chloro-2-methoxybenzoate | HCID 327084 | — |
| Reactant | HCID 178461630 | HCID 178461630 | — |
| Catalyst | Ferric acetylacetonate | HCID 5483663 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Methyl 4-ethyl-2-methoxybenzoate | HCID 23551559 | 50% |
Reaction Steps
To a solution of methyl 4-chloro-2-methoxybenzoate (example 18d) (4.16 g, 20.8 mmol) in THF (120 mL) and NMP (12 mL) was added under inert atmosphere Iron(III) acetylacetonate (398 mg, 1.17 mmol) giving a red color. Then EtMgBr (29 ml of 1M solution in ether) was added dropwise under vigorous stirring. The mixture turned dark brown and then violet and then was stirred for 15 more min. The reaction was diluted with ether and quenched upon the addition of aq. HCl (1M, 50 mL). The crude product was extracted with ether and the combined organic layers were successively washed with water and brine, dried over MgSO4, filtered and evaporated. The residue was purified on silica gel (Eluent: 30% EtOAc in hexanes) to give methyl 4-ethyl-2-methoxybenzoate (2.01 g, 50%) as an oil. 1H NMR (300 MHz, dMSO): δ 1.20-1.22 (t, 3H), 2.65-2.7 (dd, 2H), 3.9 (s, 3H), 6.8 (s, 1H), 6.97 (m, 1H), 7.7 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08784782B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-fb5580e05bc142ea94da562989fab8dc |
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| Source note | uspto-grants-2014_07 |
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