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HRID 34738作成日:2026年10月24日

Benzo(B)Thiophene → 2-(Dimethoxyacetyl)benzothiophene

https://huagongshe.com/ja/reaction/34738

反応式

関与物質

役割名称HCID仕込み量
反応物Benzo(B)ThiopheneHCID 7221—
反応物N-(dimethoxyacetyl)morpholineHCID 21298597—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Dimethoxyacetyl)benzothiopheneHCID 14276932—

反応手順

A solution of benzothiophene (7.11 g., 0.053 mol) in 120 ml. dry THF was cooled to 0°. Butyl lithium (35.3 ml. of 1.5M in hexane, 0.053 mol) was added dropwise, maintaining 0°-5°, and the mixture then warmed to ambient temperature for 1.25 hours, cooled to -75° C. and N-(dimethoxyacetyl)morpholine (10.0 g., 0.053 mol) in 50 ml. dry THF added dropwise maintaining -75° to -70°. The reaction was quenched by adding to 300 ml. saturated NH4Cl and 300 ml. ether. The organic layer was separated, washed with brine, dried over MgSO4 and stripped to an oil, 14 g., which was distilled to yield purified title product, 8.00 g., bp 137°-139°/0.25 mm.; tlc Rf 0.23 (6:1 hexane:ethyl acetate), 0.47 (2:1 hexane:ethyl acetate); 1H-nmr 3.6 (s, 6H), 5.2 (s, 1H), 7.3-7.6 (m, 2H), 7.8-8.05 (m, 2H), 8.4 (s, 1H), tlc Rf 0.31 (4:1 hexane:ethyl acetate), 0.47 (2:1 hexane:ethyl acetate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04762921
出典データセットuspto-grants-1988_08
ORD IDord-92c875558a0a424189ef189c8a798b96
出典メモuspto-grants-1988_08