戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1798578作成日:2026年10月25日

Triethylamine → 4-bromo-1-(tris(4-methoxyphenyl)methyl)-1H-pyrazole

https://huagongshe.com/reaction/1798578

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-BromopyrazoleHCID 16375—
反応物4,4',4''-Trimethoxytrityl chlorideHCID 630505—
溶媒DimethylformamideHCID 6228—
生成物4-bromo-1-(tris(4-methoxyphenyl)methyl)-1H-pyrazoleHCID 5843206652%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08343970B2
出典データセットuspto-grants-2013_01
ORD IDord-5cb637a1ff6e4359a2d949a326f74b5f
出典メモuspto-grants-2013_01