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HRID 963993作成日:2026年10月27日

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

https://huagongshe.com/reaction/963993

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物Sodium CarbonateHCID 10340—
反応物1,6-DimethoxynaphthaleneHCID 296916—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3,8-Dimethoxy-2-naphthoic acidHCID 1907903138.9%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05767116
出典データセットuspto-grants-1998_06
ORD IDord-29e77b2a28c348dd8187f35253b1a195
出典メモuspto-grants-1998_06