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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77639생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Hydrochloric AcidHCID 313—
반응물ButylamineHCID 8007—
반응물Tributyl borateHCID 12712—
반응물2,4-Pentanedione, 3-benzyl-HCID 97757—
용매Ethyl AcetateHCID 8857—
생성물4-Benzyl-1,7-diphenyl-1,6-heptadiene-3,5-dioneHCID 69501724313.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841326B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2e9fa605a42840959f88d791f2c4ede4
출처 메모uspto-grants-2014_09