反応条件: temp:-55.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: (1S,2R)-2-(Methoxycarbonyl)cyclopentanecarboxylic acid was prepared as described in J. Org. Chem. 2000, 65, 6984-6991. Tetrahydro-cyclopenta[c]furan-1,3-dione (5.0 g, 35.7 mmol) was dissolved in a 1:1 mixture of toluene and carbon tetrachloride (720 mL). The mixture was cooled to −55° C. under a nitrogen atmosphere, and then quinine (12.7 g, 39.3 mmol) was added. A solution of methanol (4.33 mL, 107 mmol) in toluene-carbon tetrachloride (1:1, 30 mL) was slowly added via an addition funnel. The suspension was stirred at −55° C. for 36 h, and then allowed to warm to 25° C. The mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate (400 mL), washed with 1.0 M aqueous hydrochloric acid solution (2×400 mL) and saturated aqueous brine solution, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo to afford the desired product, (1S,2R)-2-(methoxycarbonyl)cyclopentanecarboxylic acid (6.2 g, 35.7 mmol, quantitative), as a clear oil. 1H NMR (400 MHz, CD3OD) δ: 1.67 (1H, m), 1.84 (1H, m), 1.99 (4H, m), 3.08 (2H, m), 3.63 (3H, s).
(1S,2R)-2-(Methoxycarbonyl)cyclopentanecarboxylic acid was prepared
to warm to 25° C
The mixture was concentrated in vacuo
the residue was dissolved in ethyl acetate (400 mL)
washed with 1.0 M aqueous hydrochloric acid solution (2×400 mL) and saturated aqueous brine solution
dried over magnesium sulfate
filtered
The filtrate was concentrated in vacuo
ソース ID: ord-bcb724204a1a42a6a761bdedf6f0ce5c