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HRID 77639作成日:2026年10月23日

Benzaldehyde → 4-Benzyl-1,7-diphenyl-1,6-heptadiene-3,5-dione

https://huagongshe.com/ja/reaction/77639

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2,4-Pentanedione, 3-benzyl-HCID 97757—
溶媒Ethyl AcetateHCID 8857—
生成物4-Benzyl-1,7-diphenyl-1,6-heptadiene-3,5-dioneHCID 69501724313.8%

反応手順

Boric anhydride (0.49 g, 7.0 mmol) was combined with 3-benzyl-2,4-pentanedione (8, 1.90 g, 10.0 mmol) and stirred for 48 hr at room temperature under a nitrogen atmosphere. A solution of dry ethyl acetate (10 ml), benzaldehyde (1b, 2.05 ml, 20.2 mmol) and tributyl borate (11.0 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 filtered to afford a solid. The crude solid was triturated with methanol to give 2.30 g (63%) of a yellow solid: mp 162-164° C. [expected mp 156-158° C.]; 1H NMR: δ 3.99 (s, 2H), 6.99 (d, 2H, J=15.6 Hz), 7.34 (m, 15H), 7.77 (d, 2H, J=15.2 Hz); 13C NMR: δ 31.8, 109.3, 120.8, 126.5, 127.8, 128.1, 128.8, 130.0, 135.3, 140.5, 141.9, 183.6.

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-2e9fa605a42840959f88d791f2c4ede4
出典メモuspto-grants-2014_09