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HRID 85301作成日:2026年10月24日

Chloroform → 2-[2-(2,4,6-Trimethoxyphenyl)vinyl]thiophene

https://huagongshe.com/ja/reaction/85301

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物2,4,6-TrimethoxybenzaldehydeHCID 70019—
反応物Triphenyl(2-thienylmethyl)phosphonium BromideHCID 10741697—
反応物HCID 178506676HCID 178506676—
溶媒TetrahydrofuranHCID 8028—
生成物2-[2-(2,4,6-Trimethoxyphenyl)vinyl]thiopheneHCID 6800864992.8%

反応手順

In a stream of argon, to 30 ml of tetrahydrofuran was added 0.95 g of phenyllithium (19% solution in dibutylether) (2.15 mmol). To this mixture, 0.78 g (1.98 mmol) of thiophene-2-ylmethyltriphenylphosphonium bromide was added under cooling. After the mixture was well-stirred, 0.38 g (1.98 mmol) of 2,4,6-trimethoxybenzaldehyde dissolved in 3 ml of tetrahydrofuran was added dropwise. The mixture was reacted with stirring for 1.5 hours. After the reaction mixture was poured into 70 ml of ice water, extraction with 200 ml of chloroform, washing with a saturated saline solution, drying over anhydrous magnesium sulfate, and concentration were performed. The residue was purified by silica gel chromatography to give 508 mg (yield: 92%) of 2-[2-(2,4,6-trimethoxyphenyl)vinyl]thiophene as a colorless crystal.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846955B2
出典データセットuspto-grants-2014_09
ORD IDord-aaf7754e66d54ee3b720359ff69a7970
出典メモuspto-grants-2014_09