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HRID 751633作成日:2026年10月24日

Water → [2-(4-Methoxyphenyl)-[1,3]dioxolan-2-yl]methylamine

https://huagongshe.com/ja/reaction/751633

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium HydroxideHCID 14798—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物2-[2-(4-Methoxyphenyl)-[1,3]dioxolan-2-ylmethyl]isoindole-1,3-dioneHCID 20271801—
溶媒Diethyl EtherHCID 3283—
生成物[2-(4-Methoxyphenyl)-[1,3]dioxolan-2-yl]methylamineHCID 12833653—

反応手順

2-[2-(4-Methoxyphenyl)-[1,3]dioxolan-2-ylmethyl]isoindole-1,3-dione (Preparation 41, 2.0 g, 5.90 mmol) and hydrazine hydrate (5 mL) were combined. The stirred reaction mixture was heated under reflux for 48 h then allowed to cool to rt. Aqueous sodium hydroxide (2M, 10–15 mL) and water (20 mL) were added and the mixture stirred until a solution was formed. Diethyl ether (20 mL) was added and the biphasic mixture stirred vigorously for 16 h. The layers were separated and the aqueous layer was extracted with diethyl ether (3×20 mL), then the combined organic extracts were washed with brine (20 mL). The ethereal solution was passed through a filter paper then evaporated to dryness in vacuo to give the title compound as a yellow oil, which solidified on standing. δH (CDCl3): 1.42 (2H, br s), 3.06 (2H, s), 3.97 (3H, s), 4.00 (2H, t), 4.21 (2H, t), 7.04 (2H, d), 7.53 (2H, d).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07405210B2
出典データセットuspto-grants-2008_07
ORD IDord-7df9d0cdb3b843308e1a7c56c90e6f15
出典メモuspto-grants-2008_07