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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 229101Erstellt: 24. Oktober 2026

Methyl Acetate → (r)-2-(3-{3-[[4-Methoxy-benzyl](2,2-diphenylethyl)amino]-2-methyl-propoxy}-phenyl)acetic acid hydrochloride salt

https://huagongshe.com/de/reaction/229101

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl AcetateHCID 6584—
Edukt4-MethoxybenzaldehydeHCID 31244—
Edukt2-Chloro-3-(trifluoromethyl)benzaldehydeHCID 2736672—
EduktEther hydrochlorideHCID 10953452—
Edukt(R)-2-(3-{3-[(2,2-diphenylethyl)amino]2-methyl-propoxy}phenyl)acetic acidHCID 68862792—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(r)-2-(3-{3-[[4-Methoxy-benzyl](2,2-diphenylethyl)amino]-2-methyl-propoxy}-phenyl)acetic acid hydrochloride saltHCID 68863515—

Reaktionsschritte

Following the procedure of Example 7(d) except (R)-2-(3-{3-[(2,2-diphenylethyl)amino]2-methyl-propoxy}phenyl)acetic acid and 4-methoxybenzaldehyde were used instead of (R)-2-(3-{3-(2,2-diphenylethyl)amino]-3-methyl-propoxy}-phenyl)acetic acid methyl ester and 2-chloro-3-trifluoromethylbenzaldehyde in step (d) the corresponding carboxylic acid was obtained. The resulting amine/carboxylic acid was dissolved in Et2O (diethylether) and acidified with 1.0 M HCl/Et2O. The reaction mixture was concentrated in vacuo and dried under reduced pressure to give the title compound as a white solid, 94 mg (97%). MS (ESI) 524.4 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560586B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-44de05aac8344a81af2c8d0345dda63e
Quellennotizuspto-grants-2009_07