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HRID 76878作成日:2026年10月25日

Toluene → 3-(1-Tritylimidazol-4-YL) propionaldehyde

https://huagongshe.com/reaction/76878

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium Sodium TartrateHCID 9357—
反応物Diisobutylaluminum hydrideHCID 14487—
反応物Methyl 3-(1-Tritylimidazol-4-yl) PropionateHCID 10475868—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物3-(1-Tritylimidazol-4-YL) propionaldehydeHCID 11451428—

反応条件

温度-78 °C

反応手順

3-(1-Trityl-1H-imidazol-4-yl)propionic acid methyl ester (7.75 g, 19.5 mmol), J. Org. Chem. 2000, 65, 2229-2230, is dissolved in DCM (300 mL) and cooled to −78° C. To this is added a toluene solution of DIBAL (21.0 mL, 1.5 M). After 2 h MeOH (20 mL) is added followed by saturated aqueous Rochelle salt solution (50 mL). The mixture is partitioned between DCM and saturated aqueous Rochelle salt solution. The organic phase is dried (Na2SO4) and evaporated. The crude residue is purified via flash column chromatography (MeOH/DCM 1:99→MeOH/DCM 5:95) to give the aldehyde, 3-(1-trityl-1H-imidazol-4-yl)propionaldehyde as a yellow gum (cas #184030-88-4). 1H NMR (CDCl3) δ 9.83 (s, 1H), 7.38-7.31 (m, 10H), 7.16-7.12 (m, 6H), 6.58 (s, 1H), 2.90 (t, J=8.0 Hz, 2H), 2.83-2.79 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835646B2
出典データセットuspto-grants-2014_09
ORD IDord-be1999ba89174bc396a9555d08f6c297
出典メモuspto-grants-2014_09