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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77635생성일: 2026년 10월 23일

Benzaldehyde → Dicinnamoylmethane

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

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Hydrochloric AcidHCID 313—
반응물ButylamineHCID 8007—
반응물Tributyl borateHCID 12712—
반응물AcetylacetoneHCID 31261—
용매Ethyl AcetateHCID 8857—
생성물DicinnamoylmethaneHCID 390472162.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841326B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-998f773493e04693bd67be3f292a293a
출처 메모uspto-grants-2014_09