1-Bromoadamantane

1-Bromoadamantane
Names
	Preferred IUPAC name 1-Bromoadamantane
	Other names 1-Adamantyl bromide, adamantane, 1-bromo-, adamantyl bromide, tricyclo[3.3.1.1(3,7)]decane, 1-bromo-
Identifiers
CAS Number	768-90-1 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	1098857
ChemSpider	71437;
EC Number	230-777-3;
PubChem CID	79106;
UNII	GKV2KDH3R5 ;
	InChI InChI=1S/C10H15Br/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2 Key: VQHPRVYDKRESCL-UHFFFAOYSA-N; InChI=1/C10H15Br/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2 Key: VQHPRVYDKRESCL-UHFFFAOYAL;
	SMILES C1C2CC3CC1CC(C2)(C3)Br;
Properties
Chemical formula	C10H15Br
Molar mass	215.134 g·mol−1
Appearance	Solid
Melting point	117 °C (243 °F)
Boiling point	226 °C (439 °F)
Solubility in water	Insoluble
Hazards
NFPA 704 (fire diamond)	<imagemap> File:NFPA 704.svg\|80px\|alt=NFPA 704 four-colored diamond poly 150 150 300 300 150 450 0 300 Health 1: Exposure would cause irritation but only minor residual injury. E.g. turpentine poly 300 0 450 150 300 300 150 150 Flammability 0: Will not burn. E.g. water poly 450 150 600 300 450 450 300 300 Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen poly 300 300 450 450 300 600 150 450 Special hazards (white): no code desc none </imagemap> 1 0 0
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 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.^[1]

It reacts with phenol to give para-adamantylphenol.^[2]

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.^[3]

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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[1] 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.

[reddy-2] 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.

[3] 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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