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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530165Generated: October 25, 2026

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

https://huagongshe.com/reaction/1530165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl formateHCID 7708—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantDibenzyl 9H-fluorene-2,7-dicarboxylateHCID 66910038—
SolventTetrahydrofuranHCID 8028—
Product9-Formyl-2,7-fluorenedicarboxylic acid dibenzyl esterHCID 86609779—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090740B2
Source datasetuspto-grants-2015_07
ORD IDord-a4e984f6276243008d00e251a26118c8
Source noteuspto-grants-2015_07