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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30328Erstellt: 24. Oktober 2026

1-(Bromomethyl)-2-phenylbenzene → 2-[1,1'Biphenyl]-2-yl-1-[4-(phenylmethyl)morpholin-2-yl]-1-tetrahydro-2H-pyran-4-ylethanol

https://huagongshe.com/de/reaction/30328

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(Bromomethyl)-2-phenylbenzeneHCID 263365—
Edukt(4-benzylmorpholin-2-yl)(tetrahydro-2H-pyran-4-yl)methanoneHCID 59789303—
EduktHCID 178419666HCID 178419666—
Produkt2-[1,1'Biphenyl]-2-yl-1-[4-(phenylmethyl)morpholin-2-yl]-1-tetrahydro-2H-pyran-4-ylethanolHCID 58854907—
ProduktHCID 178419666HCID 178419666—

Reaktionsschritte

Compound 55 is prepared from 8 (0.56 g, 1.94 mmol) and 2-phenyl benzyl magnesium bromide solution (0.25 M solution in diethyl ether, 9.31 mL, 2,33 mmol, 1.2 eq) following General Procedure 2. 2-Phenylbenzyl magnesium bromide is prepared from commercially available (Aldrich) 2-phenylbenzyl bromide following General Procedure 5. Further 2-phenyl benzyl magnesium bromide solution (1 mL) is added and the reaction left under stirring overnight. Purification by ion exchange chromatography gives 55 as an off-white foam-like solid (0.37 g, 68%). MW 457.62; C30H35NO3; LCMS. (6 minute method): m/z 458 [M+H]+, RT 3.58 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423037B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-ca69a0b3786d4eeab4cf3763ad020698
Quellennotizuspto-grants-2008_09