関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chloroform | HCID 6212 | — |
| 反応物 | 2,4,6-Trimethoxybenzaldehyde | HCID 70019 | — |
| 反応物 | Triphenyl(2-thienylmethyl)phosphonium Bromide | HCID 10741697 | — |
| 反応物 | HCID 178506676 | HCID 178506676 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-[2-(2,4,6-Trimethoxyphenyl)vinyl]thiophene | HCID 68008649 | 92.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846955B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-aaf7754e66d54ee3b720359ff69a7970 |
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| 出典メモ | uspto-grants-2014_09 |
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