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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53325생성일: 2026년 10월 24일

Dimethylformamide → 3-Bromo-5-[(4-fluorophenyl)hydroxymethyl]benzaldehyde

https://huagongshe.com/ko/reaction/53325

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물1,3,5-TribromobenzeneHCID 12279—
반응물4-FluorobenzaldehydeHCID 68023—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물3-Bromo-5-[(4-fluorophenyl)hydroxymethyl]benzaldehydeHCID 1996238870.8%

반응 단계

A 2.5M solution of n-butyllithium in hexane (22.0 ml) was added dropwise to a stirred suspension of 1,3,5-tribromobenzene (15.74 g) in dry diethyl ether (500 ml) at -78° C. under an atmosphere of dry nitrogen. The resulting mixture was stirred at this temperature for 30 minutes and then 4-fluorobenzaldehyde (6.83 g) was added dropwise. Stirring at -78° C. was continued for a further 30 minutes and then another equivalent of n-butyllithium (22.0 ml of 2.5M solution in hexane) was added dropwise. The mixture was stirred at -78° C. for another 15 minutes and then N,N-dimethylformamide (15.45 g) was added. Stirring was continued for 1 hour and then water (200 ml) was added. The mixture was allowed to reach room temperature and the organic layer was separated and dried (MgSO4). Evaporation of the solvent gave an oil which was chromatographed on silica gel. Elution with dichloromethane gave impurity, and further elution with dichloromethane/methanol (99:1) gave the title compound as a gum (10.94 g), Rf 0.2 (SS 3). Found: C,53.99; H,3.41. C14H10BrFO2 requires C,54.39; H,3.26%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618941
출처 데이터셋uspto-grants-1997_04
ORD IDord-ff27c15ac276492a869dd3f5e12a61ea
출처 메모uspto-grants-1997_04