Borane;tetrahydrofuran → HCID 18177940, compound

Participants

Reaction Conditions

Reaction Steps

0.8 g of (RS)-2-(2,2,4,4-tetramethyl-chroman-6-yl)-heptanoic acid were dissolved in 15 ml THF and treated dropwise, at 0° C., with 12.3 ml of 1M BH3.THF in THF. The mixture was stirred at 0° C. for two hours and then was quenched at 0° C. with careful addition of one portion of 15 ml of 3N HCl. The mixture was stirred at room temperature for 30 min. then was extracted with three portion of 75 ml of ethyl acetate. The combined organic extracts were dried over MgSO4 and concentrated in vacuo, giving a yellow oil. The product was purified by flash chromatography (SiO2, 10% ethyl acetate/hexanes), yielding 0.5 g of a pale yellow oil. 1H NMR (CDCl3): 7.06 (d, J=2.2 Hz, 1H), 6.90 (dd, J=8.3, 2.2 Hz, 1H), 6.75 (d, J=8.3 Hz, 1H), 3.72 (dd, J=10.7, 5.7 Hz, 1H), 3.64 (dd, J=10.7, 8.0 Hz, 1H), 2.75-2.65 (m, 1H), 1.82 (s, 2H), 1.70-1.45 (m, 2H), 1.35 (s, 6H), 1.34 (s, 6H), 1.30-1.15 (m, 6H), 0.83 (t, J=6.9 Hz, 3H).

Provenance & Evidence