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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1582292Erstellt: 24. Oktober 2026

Triethylamine → 2-(2-Bromomethyl-benzyloxy)-isoindole-1,3-dione

https://huagongshe.com/de/reaction/1582292

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktN-HydroxyphthalimideHCID 10665—
Edukto-Bis(bromomethyl)benzeneHCID 66665—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(2-Bromomethyl-benzyloxy)-isoindole-1,3-dioneHCID 2198516246%

Reaktionsschritte

To a stirred solution of N-hydroxyphthalimide (0.60 g, 3.68 mmol) and Et3N (0.60 mL, 4.30 mmol) in DMF (6 mL) was added α,α′-dibromo-o-xylene (3.30 g, 0.0125 mol) and the mixture stirred at room temperature for 4 h. The resultant brown precipitate was filtered and washed with CH2Cl2. The filtrate was diluted with EtOAc (40 mL) and water (30 mL) and the organic phase washed with brine (1×30 mL), dried (Na2SO4) and concentrated under reduced pressure. The resultant yellow oil was purified by column chromatography on silica gel (4:1 Hexanes/EtOAc) to give the title compound (581 mg, 46%) as a white solid. 1H NMR (CDCl3) δ4.99 (s, 2H), 5.37 (s, 2H), 7.27-7.40 (m, 2H), 7.41-7.45 (m, 2H), 7.73-7.76 (m, 2H), 7.81-7.84 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06734191B2
Quelldatensatzuspto-grants-2004_05
ORD IDord-e1ba1fd89c434498a655f168340c1bc8
Quellennotizuspto-grants-2004_05