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(2-(Dimethylamino)ethyl)triphenylphosphonium bromide → 3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (2-(Dimethylamino)ethyl)triphenylphosphonium bromide | HCID 2724136 | — |
| 反応物 | ethyl 3-formyl-1H-indole-2-carboxylate | HCID 5107764 | — |
| 反応物 | Lithium diethylamine | HCID 45051810 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl ester | HCID 54356828 | — |
反応手順
Butyllithium (1.1 equiv.) was added to a suspension of (2-dimethylaminoethyl)triphenylphosphonium bromide in THF (0.2 M) at 0° C. After stirring for 30 minutes, lithium diethylamine (1.1 equiv.) was added dropwise followed by the cold suspension of 3-formyl-1H-indole-2-carboxylic acid ethyl ester (3.96 g, 18.2 mmol) in THF. The resulting orange suspension was stirred for 18 hours. The reaction was then quenched with saturated ammonium chloride and extracted with 10% MeOH in DCM. The organic layer was washed with saturated sodium bicarbonate, dried and concentrated to give 3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl ester as a brownish-red waxy solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06855730B2 |
| 出典データセット | uspto-grants-2005_02 |
| ORD ID | ord-bef9feba2e844741aa8e3640f2b05a5a |
| 出典メモ | uspto-grants-2005_02 |