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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 963993Erstellt: 26. Oktober 2026

Carbon Dioxide → 3,8-Dimethoxy-2-naphthoic acid

https://huagongshe.com/reaction/963993

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
EduktSodium CarbonateHCID 10340—
Edukt1,6-DimethoxynaphthaleneHCID 296916—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3,8-Dimethoxy-2-naphthoic acidHCID 1907903138,9%

Reaktionsschritte

n-Butyllithium (2.5M in hexanes; 220 ml) was added dropwise at 700° C. under nitrogen to a stirred solution of 1,6-dimethoxynaphthalene (95 g) in tetrahydrofuran (1000 ml). N, N, N', N'-Tetra-methylethylenediamine (150 ml) was added and the mixture was stirred at ambient temperature for 20 hours, then cooled to -20° C. and poured onto crushed solid carbon dioxide (500 g). When effervescence had ceased, the mixture was diluted with water (1000 ml), basified by the addition of sodium carbonate (100 g), washed with ether (2×100 ml) and acidified by the addition of concentrated hydrochloric acid. The product was extracted into ethyl acetate and the extracts were washed with brine, dried over magnesium sulphate, and the solvents removed in vacuo. The residue crystallised from ethyl acetate to give a solid which was collected by filtration, dried in vacuo, and ground to give 3,8-dimethoxy-2-naphthoic acid as a cream powder (45.6 g), m.p. 151°-153° C. Concentration of the liquor yielded a second crop of 3,8-dimethoxy-2-naphthoic acid (5.4 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05767116
Quelldatensatzuspto-grants-1998_06
ORD IDord-29e77b2a28c348dd8187f35253b1a195
Quellennotizuspto-grants-1998_06