Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39409Erstellt: 26. Oktober 2026

1,2,3-Tribromobenzene → 5-Bromo-9-isopropylidene-1,4-dihydro-1,4-methano-naphthalene

https://huagongshe.com/reaction/39409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2,3-TribromobenzeneHCID 11842—
EduktAmmonium ChlorideHCID 25517—
Edukt1,3-Cyclopentadiene, 5-(1-methylethylidene)-HCID 137467—
EduktButyllithiumHCID 178418339—
LösungsmittelTolueneHCID 1140—
Produkt5-Bromo-9-isopropylidene-1,4-dihydro-1,4-methano-naphthaleneHCID 5785760566%

Reaktionsschritte

To a stirred solution of 1,2,3-tribromo-benzene (4.34 g, 13.8 mmol) and 6,6-dimethylfulvene (2.38 g, assay 92.6%, 20.7 mmol) in dry toluene (60 ml) under a nitrogen atmosphere, 5.5 ml of a 2.5M toluene solution of n-butyllithium (14.5 mmol) were added dropwise at −5 to 0° C. within 10 minutes. After a further 10 minutes at 0° C. and 2 hours at ambient temperature, the reaction mixture was poured onto a saturated aqueous solution of ammonium chloride, extracted with ethyl acetate, washed with brine and water, dried over sodium sulphate and evaporated. Purification of the crude material on silca gel in hexane afforded 2.38 g of the desired product as a yellow oil (assay 84% by g.l.c., 55% yield). This reaction is also disclosed in WO 2007/068417.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524915B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-bc797f142524417b8cd33e6edb8dedf8
Quellennotizuspto-grants-2013_09