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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 486437Erstellt: 24. Oktober 2026

1-Bromo-3-chlorobenzene → 3-(3-Chlorophenyl)-1-(phenylmethyl)-3-piperidinol hydrochloride

https://huagongshe.com/de/reaction/486437

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-3-chlorobenzeneHCID 7928—
EduktTetrahydrofuranHCID 8028—
Edukt3-Piperidinone, 1-(phenylmethyl)-HCID 96650—
EduktMagnesiumHCID 5462224—
LösungsmittelAcetic AcidHCID 176—
Produkt3-(3-Chlorophenyl)-1-(phenylmethyl)-3-piperidinol hydrochlorideHCID 1909558676%

Reaktionsschritte

To a stirred and refluxed Grignard complex previously prepared starting from a mixture of 4.2 parts of 1-bromo-3-chlorobenzene, 5.4 parts of magnesium and 135 parts of tetrahydrofuran were added dropwise 19 parts of 1-(phenylmethyl)-3-piperidinone. Upon completion, stirring was continued for 1 hour at reflux temperature. After cooling, the reaction mixture was poured into ice water and 12.5 parts of acetic acid. The layers were separated. The aqueous phase was extracted with trichloromethane. The organic layer was washed with water, dried, filtered and evaporated. The residue was converted into the hydrochloride salt in 2-propanol. The salt was filtered off and dried, yielding 26 parts (76%) of 3-(3-chlorophenyl)-1-(phenylmethyl)-3-piperidinol hydrochloride (intermediate 27).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05292738
Quelldatensatzuspto-grants-1994_03
ORD IDord-6aaafb2e7202497f9a681d221835f2e6
Quellennotizuspto-grants-1994_03