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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30330Erstellt: 23. Oktober 2026

1-(Bromomethyl)-2-phenylbenzene → 1-[1,1'-Biphenyl]-2-yl-6,6,6-trifluoro-2-[4-(phenylmethyl)morpholin-2-yl]hexan-2-ol

https://huagongshe.com/de/reaction/30330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(Bromomethyl)-2-phenylbenzeneHCID 263365—
Edukt5,5,5-Trifluoro-1-[4-(phenylmethyl)morpholin-2-yl]pentan-1-oneHCID 59789274—
EduktHCID 178419666HCID 178419666—
Produkt1-[1,1'-Biphenyl]-2-yl-6,6,6-trifluoro-2-[4-(phenylmethyl)morpholin-2-yl]hexan-2-olHCID 5885488128%
ProduktHCID 178419666HCID 178419666—

Reaktionsschritte

Compound 67 is prepared from 10 (0.853 g, 2.71 mmol) and 2-phenyl benzyl magnesium bromide (0.25 M solution in diethyl ether, 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 is added later (19.2 mL, 4.8 mmol). Purification by automated column chromatography (eluent, EtOAc/cyclohexane 20/80 to 40/60 [v/v]), followed by ion exchange chromatography gives 67 as a viscous oil (369 mg, 28%). MW 483.58; C29H32F3NO2; LCMS: (6 min method) m/z 484 [M+H]+, RT 4.26 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423037B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-8fdb77dd934b46c0b82cea73c3125b81
Quellennotizuspto-grants-2008_09