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Triethylamine → 4-bromo-1-(tris(4-methoxyphenyl)methyl)-1H-pyrazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Bromopyrazole | HCID 16375 | — |
| 反応物 | 4,4',4''-Trimethoxytrityl chloride | HCID 630505 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-bromo-1-(tris(4-methoxyphenyl)methyl)-1H-pyrazole | HCID 58432066 | 52% |
反応手順
To a suspension of 4-bromopyrazole (1.5 g, 10.2 mmol) and 4,4′,4″-trimethoxytrityl chloride (4.5 g, 12.2 mmol) in anhydrous DMF (20 mL) under argon was added triethylamine (3 mL, 21.5 mmol) and the mixture was cooled over an ice bath. After stirring for 10 min, the ice bath was removed and the reaction stirred for 2.5 hrs. The mixture was diluted with H2O and extracted with EtOAc. The combined organics were washed with H2O three times then saturated aqueous NaHCO3 and brine. The solution was dried over Na2SO4 and concentrated in vacuo. The crude oil was recrystallized from isopropanol to give 4-bromo-1-(tris(4-methoxyphenyl)methyl)-1H-pyrazole as off-white crystals (two batches; 2.55 g, 52% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09434707B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-e22b13b5bfdd44da9a4dce6762ee6bc5 |
| 出典メモ | uspto-grants-2016_09 |