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HRID 474280作成日:2026年10月26日

Water → 2-(3,4-Dihydroxybutyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/474280

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl morpholine oxideHCID 82029—
反応物N-(3-Buten-1-yl)phthalimideHCID 339432—
触媒Osmium TetroxideHCID 30318—
溶媒TetrahydrofuranHCID 8028—
生成物2-(3,4-Dihydroxybutyl)isoindoline-1,3-dioneHCID 21592489—

反応手順

To a solution of 2-(but-3-enyl)isoindoline-1,3-dione (5.20 g, 25.8 mmol) in THF (86 mL) was added 4-methylmorpholine 4-oxide (4.54 g, 38.8 mmol) followed by osmium(VIII) oxide in water (3.16 mL, 0.517 mmol) dropwise. The reaction mixture was stirred at rt for 6 h. A saturated Na2S2SO3 solution was added to the reaction mixture and stirred for another 10 min. The aqueous layer was separated and extracted with EtOAc three times, and the combined organic layers were washed with water, brine and dried over Na2SO4. The solids were filtered off, and the filtrate was concentrated in vacuo to get 2-(3,4-dihydroxybutyl)isoindoline-1,3-dione which was used as-is in the next step. LC-MS (M+Na)+=258.1. 1H NMR (500 MHz, methanol-d4) δ 7.92-7.85 (m, 2H), 7.85-7.75 (m, 2H), 3.91-3.75 (m, 2H), 3.65 (dtd, J=9.1, 5.5, 3.7 Hz, 1H), 3.55-3.43 (m, 2H), 1.95-1.85 (m, 1H), 1.80-1.65 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637523B2
出典データセットuspto-grants-2014_01
ORD IDord-07fa7bbc91354d9d844b50e9146c33aa
出典メモuspto-grants-2014_01