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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 474280Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/474280

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl morpholine oxideHCID 82029—
EduktN-(3-Buten-1-yl)phthalimideHCID 339432—
KatalysatorOsmium TetroxideHCID 30318—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(3,4-Dihydroxybutyl)isoindoline-1,3-dioneHCID 21592489—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637523B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-07fa7bbc91354d9d844b50e9146c33aa
Quellennotizuspto-grants-2014_01