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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48550생성일: 2026년 10월 24일

3-Phenylprop-2-En-1-Ol → 3-Phenylprop-2-Enal

https://huagongshe.com/ko/reaction/48550

반응식

참여 물질

역할이름HCID투입량
반응물3-Phenylprop-2-En-1-OlHCID 308—
반응물Hydrochloric AcidHCID 313—
반응물2-NitrobenzaldehydeHCID 11101—
반응물Aluminum isopropoxideHCID 11143—
용매BenzeneHCID 241—
용매Ethyl AcetateHCID 8857—
생성물3-Phenylprop-2-EnalHCID 30798.4%

반응 단계

Cinnamyl alcohol (270 mg, 2.0 mmol) was dissolved in benzene (1 mL), added with aluminum isopropoxide (40 mg, 0.1 eq, 0.20 mmol) and 2-nitrobenzaldehyde (390 mg, 1.3 eq, 2.6 mmol) and stirred at room temperature for 1 hour. The reaction mixture was added with ethyl acetate and made acidic with addition of 2 N hydrochloric acid, and then the organic layer was separated. Subsequently, the organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated in vacuo, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1) to obtain 260 mg (yield: 97%) of the title compound as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703527B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-e0be993750554c2e8d74cf2b7b4f6647
출처 메모uspto-grants-2004_03