戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1891778作成日:2026年10月25日

Tetrahydrofuran → (5-Bromo-thiophen-2-yl)-p-tolyl-methanol

https://huagongshe.com/reaction/1891778

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物2,5-DibromothiopheneHCID 18453—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
生成物(5-Bromo-thiophen-2-yl)-p-tolyl-methanolHCID 4996286777.5%

反応条件

温度-78 °C

反応手順

To an anhydrous tetrahydrofuran (70.0 mL) solution of 2,5-dibromothiophene (5.00 g, 19.6 mmol) was added dropwise n-butyl lithium (2.55 M n-hexane solution, 7.69 mL, 19.6 mmol) on a dry ice-ethanol bath (−78° C.) under nitrogen atmosphere, which was stirred for 20 minutes at −78° C. polaldehyde (2.35 g, 19.6 mmol) was then added dropwise and stirred for 10 minutes at −78° C. The reaction mixture was allowed to room temperature and water was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:5→1:1) to obtain the tile compound (4.30 g, 77.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08507530B2
出典データセットuspto-grants-2013_08
ORD IDord-f6fb28c33fa1476f891924ef65c79bca
出典メモuspto-grants-2013_08