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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77637생성일: 2026년 10월 24일

Benzaldehyde → 2,4-Pentanedione, 3-(phenylmethylene)-

https://huagongshe.com/ko/reaction/77637

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물WaterHCID 962—
반응물AcetylacetoneHCID 31261—
촉매Acetic AcidHCID 176—
촉매PiperidineHCID 8082—
용매BenzeneHCID 241—
생성물2,4-Pentanedione, 3-(phenylmethylene)-HCID 9578295.3%

반응 단계

2,4-Pentanedione (2, 4.10 ml, 39.2 mmol) and benzaldehyde (1b, 4.06 ml, 40.0 mmol) were stirred in benzene (10 ml). Piperdine (3 drops) and glacial acetic acid (6 drops) were added and the mixture refluxed with a Dean-Stark water trap for 3 hr. The resulting mixture was cooled to room temperature, extracted into ethyl ether, washed with hydrochloric acid (1 N), saturated sodium bicarbonate, hydrochloric acid (1 N) and twice with water. The organic layer was dried over magnesium sulfate, filtered and evaporated to afford an oil. The crude oil was distilled bulb to bulb to give 7.03 g (95%) of a yellow oil; [expected mp 165-167° C.]; 1H NMR: δ 2.24 (s, 3H), 2.38 (s, 3H), 7.35 (s, 5H), 7.45 (s, 1H); 13C NMR: δ 26.5, 31.6, 128.9, 129.6, 130.5, 132.8, 139.6, 142.7, 196.2, 205.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841326B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-8755114f947d4444af80e019f14ce045
출처 메모uspto-grants-2014_09