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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1373691생성일: 2026년 10월 27일

Acetone → 2-Bromo-4-(hydroxymethyl)benzaldehyde

https://huagongshe.com/reaction/1373691

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Hydrochloric AcidHCID 313—
반응물Ethyl 3-bromo-4-cyanobenzoateHCID 18374323—
반응물DiisobutylaluminumhydrideHCID 21225700—
용매TetrahydrofuranHCID 8028—
생성물2-Bromo-4-(hydroxymethyl)benzaldehydeHCID 1837437283%

반응 단계

To a stirring cold (−78° C.) solution of ethyl 3-bromo-4-cyanobenzoate (0.41 mol, 104 g) in THF (2.3 L was added dropwise a solution of diisobutylaluminum hydride (2.0 mol, 1.36 L; 1.5 M in toluene) over a period of 1.5 h. After addition was completed, the mixture was warmed to rt over a period of 3 h. The mixture was then cooled to 0–5° C. and 40 ml of acetone was added slowly. The mixture was then transferred via a cannula to a cold (0° C.) stirring aqueous solution of HCl (2.2 L 3 N) over a period of 1.5 h, maintaining the temperature of the aqueous solution below 30° C. After the transfer was completed, the mixture was stirred for another 0.25 h. The organic solution was separated and the aqueous was extracted twice with EtOAc (3 L). The combined organic extracts were washed with brine, dried with MgSO4 (anhyd.) and concentrated to give 74 g (83%) of the title compound as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07163932B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-010c517dda5a4ba389f59be0c340c17c
출처 메모uspto-grants-2007_01