Hexane → 1-Chloro-2-(hept-1-en-6-yn-1-yl)benzene

Temperatur

0 °C

An oven-dried 250 mL three-necked round-bottomed flask under a nitrogen atmosphere was charged with 3-chlorobenzylphosphonate (3.9 g, 15 mmol) and dry THF (60 mL). The solution was cooled to 0° C. in an ice bath for 15 min, then n-BuLi (12 mL of a 1.6 M n-hexane solution, 19 mmol) was added dropwise over 10 min, via syringe. The mixture was stirred at 0° C. for 30 min, then 5-hexynal (1.0 g, 10 mmol) in dry THF (40 mL) was added. The solution was warmed to room temperature and was stirred for 3 h. The consumption of the starting material was monitored by TLC (AcOEt/n-hexane 0.5:9.5). The reaction was quenched by adding saturated aqueous ammonium chloride solution (70 mL). The layers were separated and the aqueous phase was extracted with ether (3×50 mL). The combined organic layers were washed with brine (2×50 mL), dried over Na2SO4, gravity filtered and concentrated under reduced pressure. The reaction residue was purified by silica gel flash chromatography, eluting with AcOEt/n-hexane 0.5:9.5, to provide 1.11 g of the title compound as a colorless oil in 54% yield.

1. temperatureThe solution was warmed to room temperature
2. stirringwas stirred for 3 h
3. customThe consumption of the starting material
4. customThe reaction was quenched
5. additionby adding saturated aqueous ammonium chloride solution (70 mL)
6. customThe layers were separated
7. extractionthe aqueous phase was extracted with ether (3×50 mL)
8. washThe combined organic layers were washed with brine (2×50 mL)
9. dry with materialdried over Na2SO4, gravity
10. filtrationfiltered
11. concentrationconcentrated under reduced pressure
12. customThe reaction residue was purified by silica gel flash chromatography
13. washeluting with AcOEt/n-hexane 0.5:9.5

ORD-Eintrag

ord-278db44e932546cca01128df4146d0be

Quelldatensatz

uspto-grants-2015_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09133234B2