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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 356833Erstellt: 24. Oktober 2026

N-bromobutanimide → 2-(1-Naphthyl)benzyl bromide

https://huagongshe.com/de/reaction/356833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukt(Methylphenyl)naphthaleneHCID 3016790—
KatalysatorAzobisisobutyronitrileHCID 6547—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt2-(1-Naphthyl)benzyl bromideHCID 1107733391,2%

Reaktionsschritte

114 g (0.52 mol) of 18 and 103 g (0.58 mol) of N-bromo-succinimide were dissolved in 2000 cm3 of tetrachloro-methane at room temperature, 3 g of azobisisobutyronitrile were added, and the mixture was refluxed for 4 hours. The succinimide which precipitated was filtered off, the solvent was removed in vacuo, and the residue was purified by filtration through 1000 g of silica gel (hexane/methylene chloride 9:1), giving 141 g (82%) of 19 as a colorless lachrymatory oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05840644
Quelldatensatzuspto-grants-1998_11
ORD IDord-11e0ec7f017a45db8fc648a77f1da37c
Quellennotizuspto-grants-1998_11