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HRID 888697Erstellt: 23. Oktober 2026

Benzyl formate → 9-Formyl-2,7-fluorenedicarboxylic acid dibenzyl ester

https://huagongshe.com/de/reaction/888697

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl formateHCID 7708—
EduktPotassium tert-butoxideHCID 23665647—
EduktDibenzyl 9H-fluorene-2,7-dicarboxylateHCID 66910038—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt9-Formyl-2,7-fluorenedicarboxylic acid dibenzyl esterHCID 86609779—

Reaktionsschritte

In a dry argon-purged flask, 2,7-fluorenedicarboxylic acid dibenzyl ester (3.0 g, 0.0065 mol) was dissolved in anh. THF (60 mL) at room temperature. Benzyl formate (4.2 mL, 0.035 mol, stored over anhydrous K2CO3) was added followed by addition of potassium tert-butoxide 95% (2.7 g, 0.023 mol). The reaction was stirred for three hours then the reaction was quenched with the addition of water and acidified with HCl to pH 2. The organic solvent was partially evaporated at reduced pressure. The product was twice extracted with ethyl acetate (600 mL then 200 mL). The combined organic layers were washed three times with brine, dried over sodium sulfate, filtered and evaporated to dryness. The crude product was washed with hexanes and methanol (1.9 g, 60%). 1H-NMR (d6-DMSO): δ (ppm) 11.9 (s, ˜1H, formyl); 8.8 (s, 1H, Ar); 8.5 (s, 1H, Ar); 8.4 (s, 1H, Ar); 8.2 (m, 2H, Ar); 7.9 (m, 2H, Ar); 7.5-7.4 (m, 10H, Bz); 5.4 (s, 4H, Ar).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08252275B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-77a739a595a2433d8ab7232b73530fc6
Quellennotizuspto-grants-2012_08