Names | |
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Preferred IUPAC name 1-Bromoadamantane | |
Other names 1-Adamantyl bromide, adamantane, 1-bromo-, adamantyl bromide, tricyclodecane, 1-bromo- | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
Beilstein Reference | 1098857 |
ChemSpider | |
ECHA InfoCard | 100.011.091 |
EC Number |
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PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C10H15Br |
Molar mass | 215.134 g·mol |
Appearance | Solid |
Melting point | 117 °C (243 °F) |
Boiling point | 226 °C (439 °F) |
Solubility in water | Insoluble |
Hazards | |
NFPA 704 (fire diamond) | 1 0 0 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
1-Bromoadamantane is the organobromine compound with the formula (CH2)6(CH)3CBr. A colorless solid, the compound is a derivative of adamantane with a bromine atom at one of the four equivalent methine positions.
Reactions
Although of no commercial value, 1-bromoadamantane has often been employed for testing methodology. Hydrolysis of this bromide gives the alcohol 1-hydroxyadamantane.
It reacts with phenol to give para-adamantylphenol.
Classified as a tertiary alkyl bromide, it is reluctant to form organometallic derivatives. With Rieke calcium however it forms the organocalcium derivative, which functions like a Grignard reagent.
References
- Ōsawa, Eiji (1974). "Bromination of adamantane and bicyclo(2.2.2)octane with liquid bromine". Tetrahedron Letters. 15: 115–117. doi:10.1016/S0040-4039(01)82150-X.
- V. Prakash Reddy. G. K. Surya Prakash (2003). "Electrophilic reactions of phenols". In Zvi Rappoport (ed.). The Chemistry of Phenols. PATAI'S Chemistry of Functional Groups. John Wiley & Sons. pp. 605–660. doi:10.1002/0470857277.ch9. ISBN 0471497371.
- Reuben D. Rieke; Tse-Chong Wu; Loretta I. Rieke (1995). "Highly Reactive Calcium for the Preparation of Organocalcium Reagents: 1-Adamantyl Calcium Halides and Their Addition to Ketones: 1-(1-Adamantyl)cyclohexanol". Organic Syntheses. 72: 147. doi:10.15227/orgsyn.072.0147.
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