Methyl iodide → Butyl 1-methylcyclopropane-1-sulfonate

Temperatur

0 °C

To a solution of 1-Butyl cyclopropanesulfonate (1 g, 5.58 mmol) in THF (15 ml) butyllithium solution (3.84 ml, 6.14 mmol, 1.6M, THF) was slowly added at −78° C. under nitrogen atmosphere. After 15 minutes MeI (0.72 ml, 11.16 mmol) was added and the solution was allowed to warm to 0° C. and quenched with water (1 ml). The volatiles evaporated under reduced pressure and the residue extracted with CH2Cl2 (100 ml). The extract was washed with water, dried (MgSO4) and evaporated. The residue was purified over silica gel chromatography (eluants: hexane/CH2Cl2) to obtain the titled product (0.59 g, 55.0%) as a colorless oil. 1H NMR (300 MHz, CDCl3)) δ 0.84 (m, 2H), 0.95 (t, J=7.2 Hz, 3H), 1.43 (m, 4H), 1.53 (s, 3H), 1.74(m, 2H), 4.21 ((t, J=6.6 Hz, 2H).

1. customquenched with water (1 ml)
2. customThe volatiles evaporated under reduced pressure
3. extractionthe residue extracted with CH2Cl2 (100 ml)
4. washThe extract was washed with water
5. dry with materialdried (MgSO4)
6. customevaporated
7. customThe residue was purified over silica gel chromatography (eluants: hexane/CH2Cl2)

ORD-Eintrag

ord-434b7dae4ec240f3878d9abbadcfa1c6

Quelldatensatz

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08829052B2