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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 659139Erstellt: 26. Oktober 2026

Benzaldehyde → alpha-Ethynylbenzenemethanol

https://huagongshe.com/reaction/659139

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktAmmonium ChlorideHCID 25517—
EduktHCID 178418486HCID 178418486—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-EthynylbenzenemethanolHCID 20155—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08080570B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-54eda138bf08464bbbf77e5d0f0fbb67
Quellennotizuspto-grants-2011_12