Dichloromethane → HCID 67413887, Verbindung

Temperatur

-78 °C

A 2 L, 3-necked round bottomed flask equipped with an overhead stirred was charged with 14 (67 g, 0.20 mol) and DCM (400 mL). The solution was cooled to −78° C. To this solution was slowly added boron trifluoride etherate (30 mL, 0.20 mol). The reaction mixture was stirred for 30 min. DIBAL (1 M in DCM, 600 mL, 0.6 mol) was added at a moderate rate. The solution was stirred at −78° C. for 2 h and then treated with EtOAc (100 mL) over 30 min to discharge remaining reagent. The reaction mixture was allowed to warm to −5° C. The reaction mixture was CAREFULLY quenched by the dropwise addition of 1 M HCl. The reaction mixture was diluted with DCM and H2O and made acidic to dissolve aluminum salts. The layers were separated and the organic phase was washed successively with dilute aqueous HCl, water, and brine. The DCM layer was dried over Na2SO4, filtered, and concentrated. The residue was purified by flash chromatography (SiO2, 25% to 80% EtOAc/hexane) to afford 15 as a yellow oil (36 g, 79%). [TLC analysis, 1:1 hexane/EtOAc, Rf(14)=0.8; Rf(15)=0.2]. 1H NMR (CDCl3, 300 MHz) δ5.73-5.52 (m, 2H), 4.39-4.16 (m, 1H), 4.15-4.04 (m, 2H), 3.46-3.25 (m, 2H), 2.92 (br s, 1H), 2.08-1.93 (m, 1H), 1.92-1.79 (m, 2H), 1.78-1.62 (m, 1H), 1.42 (s, 9H), ppm.

1. customA 2 L, 3-necked round bottomed flask equipped with an overhead
2. stirringThe reaction mixture was stirred for 30 min
3. stirringThe solution was stirred at −78° C. for 2 h
4. temperatureto warm to −5° C
5. customThe reaction mixture was CAREFULLY quenched by the dropwise addition of 1 M HCl
6. additionThe reaction mixture was diluted with DCM and H2O
7. dissolutionto dissolve aluminum salts
8. customThe layers were separated
9. washthe organic phase was washed successively with dilute aqueous HCl, water, and brine
10. dry with materialThe DCM layer was dried over Na2SO4
11. filtrationfiltered
12. concentrationconcentrated
13. customThe residue was purified by flash chromatography (SiO2, 25% to 80% EtOAc/hexane)

ORD-Eintrag

ord-88537c54943c470599e80135de489ee6

Quelldatensatz

uspto-grants-2009_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07517906B2