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HRID 34745作成日:2026年10月25日

3-Bromoquinoline → 3-(Dimethoxyacetyl)quinoline

https://huagongshe.com/reaction/34745

反応式

関与物質

役割名称HCID仕込み量
反応物3-BromoquinolineHCID 21413—
反応物N-(dimethoxyacetyl)morpholineHCID 21298597—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物3-(Dimethoxyacetyl)quinolineHCID 14276934—

反応手順

3-Bromoquinoline (3.29 ml., 0.032 mol) was dissolved in 300 ml. THF and cooled to -78°. n-Butyllithium (13.6 ml. of 2.5M in hexane, 0.034 ml.) was added slowly and the mixture stirred 15 minutes at -75° to -78°. N-(Dimethoxyacetyl)morpholine (5.98 g., 0.032 mol) in 10 ml. THF was then added and stirring continued for 1.75 hours at the same temperature. The reaction was then quenched into 300 ml. saturated NH4Cl. The aqueous layer was separated and extracted 4×100 ml. ether. The organic layers were combined, dried over MgSO4, stripped to yield title product, 7.0 g., bp 120°-123°/0.125 torr.

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-97c01dee82af4b81ba08bf372d90172a
出典メモuspto-grants-1988_08