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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 659139생성일: 2026년 10월 26일

Benzaldehyde → alpha-Ethynylbenzenemethanol

https://huagongshe.com/reaction/659139

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Ammonium ChlorideHCID 25517—
반응물HCID 178418486HCID 178418486—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물alpha-EthynylbenzenemethanolHCID 20155—

반응 단계

To a solution of 2.65 g of benzaldehyde (Formula 26) in 50 mL of THF at room temperature was added 100 mL of 0.5M ethynylmagnesium bromide in THF. The mixture was stirred at room temperature for 2 hours. Then, the mixture was diluted with diethylether and a saturated solution of ammonium chloride. The mixture was extracted with ethyl acetate. Combined ethyl acetate was washed with brine, dried over sodium sulfate and concentrated. Column chromatography (20% ethyl acetate/hexane) gave 3.17 g of 1-phenyl-prop-2-yn-1-ol (Formula 27) as a light yellow oil. 1H NMR (300 MHz, CDCl3) δ 2.68 (m, 1H), 5.46-5.49 (m, 1H), 7.34-7.43 (m, 3H), 7.55-7.57 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08080570B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-54eda138bf08464bbbf77e5d0f0fbb67
출처 메모uspto-grants-2011_12