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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 983764생성일: 2026년 10월 24일

Benzaldehyde → 1-Phenylbut-3-en-1-ol

https://huagongshe.com/ko/reaction/983764

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Hydrochloric AcidHCID 313—
반응물Allyl bromideHCID 7841—
반응물HCID 178418365HCID 178418365—
촉매HCID 178460666HCID 178460666—
용매Diethyl EtherHCID 3283—
생성물1-Phenylbut-3-en-1-olHCID 22011994%

반응 단계

To 0.30 ml (1.0 mmol) of tetraisopropoxytitanium and 5 ml of ethyl ether solution containing allyl bromide (1.0 mmol) was added dropwise at −50° C. 1.67 ml of 1.2M ethyl ether solution containing isopropylmagnesium bromide (2.0 mmol). Upon stirring at −50° C. to −40° C. for 1 hour, the reaction liquid turned from yellow into brown. To the reaction liquid was added 0.071 ml (0.7 mmol) of benzaldehyde at −45° C. to −40° C. The temperature was raised to −10° C. to 0° C. over 30 minutes. With 5 ml of 1N hydrochloric acid added, the solution was heated to room temperature and separated into layers. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate. After drying with anhydrous magnesium sulfate, the solution was freed of solvent by vacuum distillation. The residues were purified by silica gel chromatography. Thus there was obtained 97 mg of 1-phenyl-3-buten-1-ol (94% yields based on benzaldehyde).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06867161B1
출처 데이터셋uspto-grants-2005_03
ORD IDord-da80cfd320f547a29825db22460bf3d6
출처 메모uspto-grants-2005_03