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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39409Generated: October 24, 2026

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

https://huagongshe.com/en/reaction/39409

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3-TribromobenzeneHCID 11842—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,3-Cyclopentadiene, 5-(1-methylethylidene)-HCID 137467—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
Product5-Bromo-9-isopropylidene-1,4-dihydro-1,4-methano-naphthaleneHCID 5785760566%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524915B2
Source datasetuspto-grants-2013_09
ORD IDord-bc797f142524417b8cd33e6edb8dedf8
Source noteuspto-grants-2013_09