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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17100Erstellt: 24. Oktober 2026

Trifluoroacetic acid → 2-((6-Bromopyridin-2-yl)methyl)isoindoline-1,3-dione

https://huagongshe.com/de/reaction/17100

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktPhthalimideHCID 6809—
EduktTriphenylphosphineHCID 11776—
Edukt1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Edukt(6-Bromopyridin-2-yl)methanolHCID 3517811—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-((6-Bromopyridin-2-yl)methyl)isoindoline-1,3-dioneHCID 22176446—

Reaktionsschritte

A mixture of commercially available (6-bromopyridin-2-yl)methanol (20.0 g, 0.106 mol), phthalimide (20.4 g, 0.138 mol), and triphenylphosphine (36.2 g, 0.138 mol), and 1,1′-(azodicarbonyl)-dipiperidine (34.8 g, 0.138 mol) in anhydrous tetrahydrofuran (1 L) was stirred at room temperature overnight. The precipitate was collected by vacuum filtration and washed with tetrahydrofuran. The filtrate was concentrated under reduced pressure, and the solid residue was triturated with methanol with sonication. A214.1 was collected by vacuum filtration and was dried well to give 24.1 g as a white solid. The filtrate still contained significant product which could be isolated as a second crop with methanol trituration. The compound had an HPLC retention time=2.32 min. (Column: Chromolith SpeedROD 4.6×50 mm—4 min.; Solvent A=10% MeOH, 90% H2O, and 0.1% TFA; Solvent B=90% MeOH, 10% H2O, and 0.1% TFA) and a LC/MS M+1=317.15 and 319.15.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737279B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-b3467d2092bb4e8c87455c945af69572
Quellennotizuspto-grants-2010_06