戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 77635作成日:2026年10月24日

Benzaldehyde → Dicinnamoylmethane

https://huagongshe.com/ja/reaction/77635

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Hydrochloric AcidHCID 313—
反応物ButylamineHCID 8007—
反応物Tributyl borateHCID 12712—
反応物AcetylacetoneHCID 31261—
溶媒Ethyl AcetateHCID 8857—
生成物DicinnamoylmethaneHCID 390472162.8%

反応手順

Boric anhydride (0.49 g, 7.0 mmol) was combined with 2,4-pentanedione (2, 1.05 ml, 10.0 mmol) and stirred for 18 hr at room temperature under a nitrogen atmosphere. A solution of dry ethyl acetate (10 ml), benzaldehyde (1b, 2.05 g, 20.2 mmol) and tributyl borate (11.00 ml, 40.5 mmol) was added and the mixture stirred for 15 min at room temperature. Butylamine (0.20 ml, 2.0 mmol) was added dropwise over 30 min and stirring was continued for 18 hr at room temperature. Hydrochloric acid (15 ml, 0.4 N) was warmed to 60° C., added to the mixture and stirring was continued for 1 hr. The resulting mixture was extracted into ethyl acetate, washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to afford a solid. The crude solid was triturated with methanol to give 0.90 g (33%) of a yellow solid: mp 140-142° C. [expected mp 139-140° C.]; 1H NMR: δ 5.84 (s, 1H), 6.62 (d, 2H, J=15.7 Hz), 7.39 (m, 6H), 7.54 (dd, 4H, J=7.4, 4.0 Hz), 7.66 (d, 2H, J=15.9 Hz), 15.85 (s, 1H); 13C NMR: δ 101.6, 124.1, 128.0, 128.9, 130.0, 135.0, 140.5, 183.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841326B2
出典データセットuspto-grants-2014_09
ORD IDord-998f773493e04693bd67be3f292a293a
出典メモuspto-grants-2014_09