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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231355Erstellt: 25. Oktober 2026

Carbon Dioxide → 2,6-Dimethoxybenzoic Acid

https://huagongshe.com/reaction/231355

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
Edukt1,3-DimethoxybenzeneHCID 9025—
EduktPotassium diethylamideHCID 12552075—
LösungsmittelWaterHCID 962—
LösungsmittelTriethylamineHCID 8471—
Produkt2,6-Dimethoxybenzoic AcidHCID 1510969%

Reaktionsschritte

A solution of 1,3-dimethoxybenzene (12.06 g.) and tetramethylethylenediamine (15 ml.) in triethylamine (20 ml.) was added to the potassium diethylamide reaction mixture and stirred for two hours. The entire mixture, a gray suspension, was poured into a 1-liter beaker containing crushed dry ice (456 g.) with the aid of 35 ml of added triethylamine and was allowed to warm to room temperature. The contents of the beaker were transferred into a 1-liter flask with the aid of some water. All volatile components were removed by a rotary evaporator. The solid remaining in the flask was partitioned between diethyl ether (30 ml.) and water, which was extracted with diethyl ether (four times, 30 ml.). The aqueous layer was acidified with concentrated hydrochloric acid to a pH of 1. The resultant precipitate was collected by filtration, water-washed and air dried to give 10.99 g. (69% yield) of 2,6-dimethoxybenzoic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04845276
Quelldatensatzuspto-grants-1989_07
ORD IDord-099de03743944935877b63130f78306e
Quellennotizuspto-grants-1989_07