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Sodium bis(trimethylsilyl)amide → 4-(2,3-Dihydro-1-benzofuran-7-yl)but-3-enoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| 反応物 | (2-Carboxyethyl)triphenylphosphonium bromide | HCID 2733850 | — |
| 反応物 | 2,3-Dihydro-1-benzofuran-7-carbaldehyde | HCID 2795018 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-(2,3-Dihydro-1-benzofuran-7-yl)but-3-enoic acid | HCID 123771320 | — |
反応手順
To a solution of (2-carboxyethyl)triphenylphosphonium bromide (617 mg, 1.5 mmol) in THF (20 mL) was added NaHMDS (1.5 mL, 3.0 mmol) at −20° C., and the reaction was stirred for 20 min. 2,3-Dihydro-1-benzofuran-7-carbaldehyde (200 mg, 1.4 mmol) was added to the reaction at −78° C., and the reaction was stirred overnight while warming to rt. The reaction was diluted with water (30 mL) and extracted with EtOAc (3×30 mL). Organics were washed with brine (30 mL), dried (Na2SO4), and concentrated to give the crude title compound as a yellow solid. [M+H] Calc'd for C12H12O3, 205. Found, 205.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09447046B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-24cb8016109040e7982e82072fc4a763 |
| 出典メモ | uspto-grants-2016_09 |