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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41374Generated: October 27, 2026

Carbon Dioxide → 5-Ethyl-2-methoxybenzoic acid

https://huagongshe.com/reaction/41374

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 numberUS08530469B2
Source datasetuspto-grants-2013_09
ORD IDord-586c5c68ab78400ea353a5ec93d7a354
Source noteuspto-grants-2013_09