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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-chloro-2-methoxybenzoateHCID 327084—
ReactantHCID 178461630HCID 178461630—
CatalystFerric acetylacetonateHCID 5483663—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductMethyl 4-ethyl-2-methoxybenzoateHCID 2355155950%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08784782B2
Source datasetuspto-grants-2014_07
ORD IDord-fb5580e05bc142ea94da562989fab8dc
Source noteuspto-grants-2014_07