戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7462作成日:2026年10月23日

Water → 5-[2-(3-Bromopropoxy)ethyl]-1-benzothiophene

https://huagongshe.com/ja/reaction/7462

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Carbon tetrabromideHCID 11205—
反応物TriphenylphosphineHCID 11776—
反応物3-[2-(1-Benzothiophen-5-yl)ethoxy]-1-propanolHCID 21990066—
溶媒DichloromethaneHCID 6344—
生成物5-[2-(3-Bromopropoxy)ethyl]-1-benzothiopheneHCID 2199007676.2%

反応手順

In 40 mL of methylene chloride was dissolved 2.00 g of 3-[2-(1-benzothiophen-5-yl)ethoxy]-1-propanol, and 5.55 g of triphenylphosphine was added to the solution, after which a solution of 8.42 g of carbon tetrabromide in 10 mL of methylene chloride was added dropwise thereto under ice-cooling and the resulting mixture was stirred at room temperature for 20 minutes. To the reaction mixture was added 20 mL of water, and the organic layer was separated. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. Diethyl ether was added to the residue and the insoluble materials were filtered off, after which the solvent was distilled off under reduced pressure. The residue was purified by a column chromatography (eluent; hexane:ethyl acetate=20:1 to 10:1) to obtain 1.93 g of 5-[2-(3-bromopropoxy)ethyl]-1-benzothiophene as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087594B2
出典データセットuspto-grants-2006_08
ORD IDord-955645a8fc6a4fd1b0144ff9ec621f18
出典メモuspto-grants-2006_08