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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334873Generated: October 29, 2026

Carbon Dioxide → 5-Ethyl-2-methoxybenzoic acid

https://huagongshe.com/reaction/334873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantSodium HydroxideHCID 14798—
Reactant1-Ethyl-4-methoxybenzeneHCID 73690—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product5-Ethyl-2-methoxybenzoic acidHCID 2072114937%

Reaction Steps

n-Butyl lithium (2.5M in hexanes, 38.5 ml, 100.0 mmol) was added dropwise under a nitrogen atomosphere to a stirred solution of 4-ethylanisole (11.7 g, 86.0 mmol) and N,N,N′,N′-tetramethylethylenediamine (10 ml, 88.0 mmol) in anhydrous diethyl ether (100 ml) and the mixture was stirred and held at 30° C. for 16 hours. The mixture was cooled and poured slowly in to a mixture of excess solid carbon dioxide in anhydrous diethyl ether. Upon warming to room temperature the mixture was made basic by the addition of 2M sodium hydroxide, the aqueous layer was separated and acidified to pH 2 or below by the addition of concentrated hydrochloric acid. The mixture was extracted with diethyl ether, the organic layer separated and the solvent removed in vacuo to afford 5-ethyl-2-methoxybenzoic acid (5.7 g, 37%) as a pale yellow oil. 1H NMR (DMSO-d6) 12.50 (1H, br s), 7.48 (1H, d), 7.33 (1H, dd), 7.03 (1H, d), 2.56 (2H, q), 1.17 (3H, q). MS: [M+H]+ 181.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883790B2
Source datasetuspto-grants-2014_11
ORD IDord-34b8160c78384315b830d16869aee945
Source noteuspto-grants-2014_11