Molecules 2001, 6, M239

Molecules 2001, 6, M239

4,7,7-Trimethyl-bicyclo [2.2.1]heptan-2-ol

Badia Ait Allal, Larbi El Firdoussi, Smail Allaoud and Abdellah Karim

Laboratoire de Chimie de Coordination Faculté des Sciences SemLalia, BP 2390 Marrakech Maroc. Fax: 212 44 43 74 08, E-mail: [email protected]

Received: 10 January 2001 / Accepted: 15 May 2001 / Published: 25 May 2001

A mixture of Pd(acac)₂ (41.26 mg, 0.12 mmol) and CuCl₂ (168 mg, 1.25 mmol) [1] in 10 mL of 1,2-dimethoxyethan (DME) was stirred for 30 mn at 80°C under oxygen atmosphere, was added a -pinene (425 mg, 3.12 mmol). The mixture was stirred for another 18h at he same temperature. The evolution of reaction was controlled by GC. When the reaction was completed, 5mL of water and hexane/EtOAc (1:1, 20 mL) were added. The phases were separated and the aqueous one was extracted with hexane/EtOAc (1:1, 4x20mL), and the combined organic phases were washed with water, dried over MgSO₄. Removal of the solvent under reduced pressure and purification of the residue by flash chromatography, using hexane as eluent, gave the compound 2 (45%) as a colorless oil [2].

¹H NMR (300MHz, CDCl₃) 0.87(6H; 8-Me and 9-Me) 0.92(s; 3H; 10-Me) 1.30(3H, m) 1.70(2H, m) 2,06(1H, m) 2.45(1H, m, 1-CH) 4.16(1H, ddd; J_{2ax, 3ax}10.8 J_{2ax, 1eq}4.2 J_{2ax, 3eq}2.4Hz, 2-CH).

¹³C NMR (75MHz, CDCl₃) 13.27(CH₃, C-10); 18.48 and 20.58 (CH₃, C-8 and C-9) 28.03 and 28.12 (CH₂, C-6 and C-5) 40.16 (CH₂, C-3) 44.92 (CH, C-1) 47.86 (quat, C-7) 50.83(quat, C-4); 68.01(CH, C-2).

References

1. EL Firdoussi, L.; Baqqa A.; Allaoud, S.; Aitallal, B.; Karim, A.; Castanet, Y.; Mortreux, A. J. Mol. Cat. 1998, 135, 11.
2. Bohlmann, F.; Zeisberg, R. Organic Magnetic Resonance1975, 7, 426.

Sample Availability: Available from the authors and from MDPI.