化工社化工社 化学情報印刷レポート · 研究参考用
2-Bromothiazole → (3-Bromo-2-fluorophenyl)(thiazol-2-yl)methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Bromothiazole | HCID 76430 | — |
| 反応物 | 3-Bromo-2-fluorobenzaldehyde | HCID 22019361 | — |
| 反応物 | HCID 178418918 | HCID 178418918 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (3-Bromo-2-fluorophenyl)(thiazol-2-yl)methanol | HCID 86730392 | — |
反応手順
To a solution of 2-bromothiazole (0.088 mL, 0.985 mmol) in THF (2.99 mL) cooled to 0° C. was added isopropylmagnesium chloride (0.493 mL, 0.985 mmol). After 50 min, 3-bromo-2-fluorobenzaldehyde (0.200 g, 0.985 mmol) was added. The reaction mixture was allowed to warm to room temperature overnight. After 12 hr, the reaction was quenched with saturated aqueous NH4Cl. The reaction mixture was diluted with CH2Cl2. The layers were separated. The aqueous phase was extracted with CH2Cl2 (2×). The organic phases were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a brown liquid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09242967B2 |
| 出典データセット | uspto-grants-2016_01 |
| ORD ID | ord-2b6f271362fe4e7ba61a23ffd2bf98ee |
| 出典メモ | uspto-grants-2016_01 |