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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1691156Erstellt: 27. Oktober 2026

N-Formylmorpholine → 4-(Phenoxymethyl)benzaldehyde

https://huagongshe.com/reaction/1691156

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-FormylmorpholineHCID 20417—
Edukt1-Bromo-4-(phenoxymethyl)benzeneHCID 726149—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(Phenoxymethyl)benzaldehydeHCID 12106287100,6%

Reaktionsbedingungen

Temperatur78 °C

Reaktionsschritte

To a tetrahydrofuran solution (50 mL) of 1-bromo-4-phenoxymethyl-benzene (4.69 g, 17.8 mmol) described in Manufacturing Example 86-1-1 was added dropwise n-butyl lithium (16.8 mL, 1.59 M hexane solution, 26.7 mmol) at −78° C. After 40 minutes of stirring at 78° C., N-formylmorpholine (2.25 g, 19.6 mmol) was added to this mixture, which was then stirred for a further 30 minutes at that temperature. This mixture was partitioned into diethyl ether and water. The organic layer was separated, washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (3.8 g). This compound was used in the subsequent reaction without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08153662B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-7d7ef1525c574f3aa00d4ad7c2e772a9
Quellennotizuspto-grants-2012_04