in hexane; cyclohexane
1-bromooctane (1 equiv.) and TMTH (2 equiv.) in hexane cooled to 0°C under Ar, LDA (1 equiv., 1.6 M soln. in cyclohexane) dropped in, stirred for 20-25 min at room temp., quenched with water; analyzed by GC (after quenching), NMR (before quenching);
参考文献
Reimann, Werner; Kuivila, Henry G.; Farah, Dan; Apoussidis, Theodorus
Organometallics, 1987 , vol. 6, p. 557 - 565
in tetrahydrofuran
TMTH (1.10 mmol) and 1-bromooctane (1.10 mmol) in THF cooled to 0°C under Ar, MeLi (1.10 mmol) in THF added, stirred for 15 min at room temp., hydrolyzed with water; H2 collected with gas measuring device, GC analysis of org. layer;
参考文献
Reimann, Werner; Kuivila, Henry G.; Farah, Dan; Apoussidis, Theodorus
Organometallics, 1987 , vol. 6, p. 557 - 565
in diethyl ether; hexane; cyclohexane
LiH and Sn2Me6 prepared in situ from TMTH (2.00 mmol) and LDA (1.00 mmol, 1.60 M in cyclohexane) in hexane under Ar, after addn. of Et2O and stirring for 2 h at room temp. treated with 1-bromooctane (1.00 mmol), stirred for 15 min, quenched with water; analyzed by GC;
参考文献
Reimann, Werner; Kuivila, Henry G.; Farah, Dan; Apoussidis, Theodorus
Organometallics, 1987 , vol. 6, p. 557 - 565
