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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644587Generated: October 29, 2026

Carbon Dioxide → 5-Ethyl-2-methoxybenzoic acid

https://huagongshe.com/reaction/644587

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 numberUS07700625B2
Source datasetuspto-grants-2010_04
ORD IDord-814c8e83ecea4378a20df35931477cdb
Source noteuspto-grants-2010_04