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HRID 1048819作成日:2026年10月26日

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

https://huagongshe.com/reaction/1048819

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl formateHCID 7708—
反応物Potassium tert-butoxideHCID 23665647—
反応物Dibenzyl 9H-fluorene-2,7-dicarboxylateHCID 66910038—
溶媒TetrahydrofuranHCID 8028—
生成物9-Formyl-2,7-fluorenedicarboxylic acid dibenzyl esterHCID 86609779—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09381254B2
出典データセットuspto-grants-2016_07
ORD IDord-fab7959bca8a4b86bd69d57afa14522d
出典メモuspto-grants-2016_07