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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412142Generated: October 31, 2026

Carbon Dioxide → 5-Ethyl-2-methoxybenzoic acid

https://huagongshe.com/reaction/2412142

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 atmosphere 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 numberUS08816087B2
Source datasetuspto-grants-2014_08
ORD IDord-a867d77ef94e4676b3f146a3c5e199e6
Source noteuspto-grants-2014_08