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HRID 1245562作成日:2026年10月26日

Benzene → Dibenzyl ethylmalonate

https://huagongshe.com/reaction/1245562

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物Benzyl BromideHCID 7498—
反応物Ethylmalonic acidHCID 11756—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
生成物Dibenzyl ethylmalonateHCID 53752489—

反応手順

A solution of 2.0 g (15 mmol) of ethyl-malonic acid, 4.7 mL (31 mmol) of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) and 3.9 mL (32 mmol) of benzyl bromide in 100 mL of benzene was refluxed for 22 hours. After cooling, the reaction was washed with 150 mL of H2O. After separating layers, the organic phase was dried over MgSO4 and concentrated. The residue was purified on a 40M Biotage column using 24:1 v/v hexane/EtOAc as the eluant to afford the title compound as a colorless oil: RF: 0.40 (9:1 v/v hexane/EtOAc); 1H-NMR (500 MHz) δ 0.97 (t, J=7.4, 3H), 1.99 (quint, J=7.4, 2H), 3.39 (t, J=7.4, 1H), 5.17 (s, 2H), 7.29–7.36 (m, 10H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07125887B2
出典データセットuspto-grants-2006_10
ORD IDord-a9ef386b9fb540bf93afcf5cc3ee8541
出典メモuspto-grants-2006_10