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HRID 2209464作成日:2026年10月27日

Methanol → HCID 54509567、化合物

https://huagongshe.com/reaction/2209464

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物3-Nitrophenylboronic AcidHCID 1677—
反応物Sodium CarbonateHCID 10340—
反応物2-bromo-4-(4-pyridinylmethyl)BenzenamineHCID 21865645—
溶媒BenzeneHCID 241—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
溶媒AluminumHCID 5359268—
生成物HCID 54509567HCID 5450956785.3%

反応手順

4-(4-Amino-3-bromobenzyl)pyridine (1.0 gm), 3-nitrobenzene boronic acid (0.63 gm), palladium tetrakis triphenylphosphine (0.47 gm), methanol (6.5 mL), 2.0M Na2CO3 (1.9 mL) and benzene (32 mL) are combined in a reaction flask that is wrapped in aluminum foil (to prevent exposure of the reagents to light). The reaction mixture is heated to reflux for 6 hours. The progress of the reaction is monitored by thin-layer chromatography (9:1 hexane:ethyl acetate). When the starting material is converted, the reaction mixture is allowed to cool and the solvents are removed. Ethyl acetate is added to the residue, the resultant solution is filtered through a pad of Na2SO4, and concentrated. The product is isolated by preparative thin-layer chromatography (9:1 hexane:ethyl acetate) yielding 983 mg of 4-[4-amino-3-(3-nitrophenyl)benzyl]pyridine as an orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05455252
出典データセットuspto-grants-1995_10
ORD IDord-81a3102cb48e4c0b8237898f90eb372f
出典メモuspto-grants-1995_10