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HRID 40948作成日:2026年10月25日

Ethanol → 4-Bromo-2-(diethoxymethyl)thiophene

https://huagongshe.com/reaction/40948

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Ammonium ChlorideHCID 25517—
反応物4-Bromothiophene-2-carbaldehydeHCID 87792—
反応物EthylorthoformateHCID 53630039—
生成物4-Bromo-2-(diethoxymethyl)thiopheneHCID 1228002481%

反応条件

温度60 °C

反応手順

A mixture of 4-bromothiophene-2-carbaldehyde (1.2 g, 0.0063 mol) in ethanol (10 mL, 0.2 mol) was treated with ammonium chloride (0.42 g, 0.0078 mol) and ethyl orthoformate (1.2 g, 0.0078 mol). The mixture was stirred at 60° C. for 2 hours. The reaction was quenched with water and extracted with ethyl acetate. The combined organic layer was washed with saturated sodium chloride, dried over magnesium sulfate, filtered and concentrated to give 4-bromo-2-(diethoxymethyl)thiophene as an oil (1.3 g, 81%). 1H NMR (400 MHz, CDCl3): δ□ 7.22 (s, 1H), 6.99 (s, 1H), 5.68 (s, 1H), 3.63 (q, 4H) 1.24 (t, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530485B2
出典データセットuspto-grants-2013_09
ORD IDord-9c7dc7f272d74b8fa26ea2c736107aea
出典メモuspto-grants-2013_09