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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1194027Erstellt: 26. Oktober 2026

Water → (1-{[(3-Phenoxyphenyl)methoxy]methyl}cyclopropyl)methanol

https://huagongshe.com/reaction/1194027

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt1-(Bromomethyl)-3-phenoxybenzeneHCID 94544—
Edukt1,1-Bis(hydroxymethyl)cyclopropaneHCID 4101437—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(1-{[(3-Phenoxyphenyl)methoxy]methyl}cyclopropyl)methanolHCID 1384940640,5%

Reaktionsschritte

A solution of 1,1-dihydroxymethylcyclopropane (3 g) in tetrahydrofuran (20 cm3) was added dropwise to a suspension of sodium hydride (0.35 g) in tetrahydrofuran (30 cm3). After effervescence has ceased, tetrabutylammonium iodide (1 g) was added to the grey suspension followed by a solution of 3-phenoxybenzyl bromide (3.88 g) in tetrahydrofuran (15 cm3) at the ambient temperature and the mixture stirred for a further 2 hours. The mixture was poured into water and extracted with ethylacetate. The extracts were combined, dried over magnesium sulphate and concentrated by evaporation of the solvent, and the residual oil purified by column chromatography using a silica gel column eluting first with dichloromethane, followed then by ethylacetate, to give 1-hydroxymethyl-1-(3-phenoxybenzyloxymethyl)cyclopropane (1.7 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04812483
Quelldatensatzuspto-grants-1989_03
ORD IDord-79fa025abbde4ca799c4dc894185ef47
Quellennotizuspto-grants-1989_03