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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2,3-Tribromobenzene | HCID 11842 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1,3-Cyclopentadiene, 5-(1-methylethylidene)- | HCID 137467 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Bromo-9-isopropylidene-1,4-dihydro-1,4-methano-naphthalene | HCID 57857605 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524915B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-bc797f142524417b8cd33e6edb8dedf8 |
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| Source note | uspto-grants-2013_09 |
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