Hydrochloric Acid → 5-bromo-1-(1,3-dithian-2-yl)-2,3-dihydro-1H-inden-1-ol

Temperatur

-15 °C

To a solution of 1,3-dithiane (1.82 g, 14.7 mmol) in dry THF (20 ml) was added n-butyllithium (8.62 ml, 13.8 mmol, 1.6 M in hexane) dropwise at −30° C. The resulting mixture was stirred for 2 h at −15° C. Then, a solution of 5-bromo-2,3-dihydro-1H-inden-1-one (2 g, 9.19 mmol) in dry THF (24 ml) was added dropwise, maintaining the temperature between −15° C. and −6° C. After the addition was completed, the brown solution was allowed to warm to 0° C. and was then stored in the fridge overnight. Then, 1N HCl was added and the brown mixture was extracted two times with diethylether. The combined organic layers were washed with brine, dried with Na2SO4 and evaporated. The remaining residue was purified by chromatography (silica gel; heptane/EtOAc 90:10-75:25) to obtain the title compound as light yellow gum (2.167 g, 71%). MS: 330.1 [M+H]+.

1. temperaturemaintaining the temperature between −15° C. and −6° C
2. additionAfter the addition
3. temperatureto warm to 0° C.
4. customwas then stored in the fridge overnight
5. extractionthe brown mixture was extracted two times with diethylether
6. washThe combined organic layers were washed with brine
7. dry with materialdried with Na2SO4
8. customevaporated
9. customThe remaining residue was purified by chromatography (silica gel; heptane/EtOAc 90:10-75:25)

ORD-Eintrag

ord-2267c5a4830640a0830f5cba6c1dc3d5

Quelldatensatz

uspto-grants-2013_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08592426B2