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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662567생성일: 2026년 10월 24일

3-Benzyloxybenzaldehyde → 1-(3-(Benzyloxy)phenyl)but-2-yn-1-ol

https://huagongshe.com/ko/reaction/1662567

반응식

참여 물질

역할이름HCID투입량
반응물3-BenzyloxybenzaldehydeHCID 74342—
반응물HCID 178419101HCID 178419101—
용매TetrahydrofuranHCID 8028—
생성물1-(3-(Benzyloxy)phenyl)but-2-yn-1-olHCID 5770599297.2%

반응 조건

온도-78 °C

반응 단계

A 1 L round bottom flask was charged with 1-propynylmagnesium bromide (0.5 M in THF) (available from Aldrich) (245 mL, 123 mmol) and cooled to −78° C. To the cold slurry was added a solution of 3-benzyloxybenzaldehyde (available from Aldrich) (20.0 g, 94.2 mmol) in THF (30 mL) over 15 minutes. The mixture was stirred for 30 minutes at −78° C., the cooling bath was removed, and stirring was continued for 1 hour at ambient temperature. The reaction was quenched with saturated aqueous ammonium chloride and diluted with EtOAc. The organics were washed with water and brine, dried (MgSO4), and concentrated. The crude product was purified by silica gel flash chromatography (0-30% EtOAc/hexane) to afford 93.A (23.1 g, 97% yield) as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08030354B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-2f4894906a1b460db637c4867fb09e6e
출처 메모uspto-grants-2011_10