Water → 2-Isopropylpyridine

Temperature

-20 °C

A solution of 19.4 ml (0.17 mol) of 2-ethylpyridine in 100 ml of tetrahydrofuran was cooled to −20° C. and 125 ml of n-butyllithium (1.6M in hexane, 0.2 mol) were subsequently added while stirring. The mixture was allowed to come to room temperature, stirred for another one hour and subsequently cooled back down to −20° C. A solution of 18 ml (0.25 mol) of methyl iodide in 20 ml of tetrahydrofuran was then added at such a rate that the temperature remained at −20° C. The mixture was allowed to warm to room temperature, stirred for a further 14 hours and hydrolyzed with 60 ml of water. The organic phase was separated off and the aqueous phase was extracted three times with 50 ml each time of diethyl ether. The organic phases were combined, dried over magnesium sulfate, the magnesium sulfate was filtered off and the solvent was distilled off. The residue obtained in this way was distilled at 81-84° C./60 torr. This gave 10.88 g (53%) of 2-isopropylpyridine.

1. customto come to room temperature
2. stirringstirred for another one hour
3. customremained at −20° C
4. temperatureto warm to room temperature
5. customThe organic phase was separated off
6. extractionthe aqueous phase was extracted three times with 50 ml each time of diethyl ether
7. dry with materialdried over magnesium sulfate
8. filtrationthe magnesium sulfate was filtered off
9. distillationthe solvent was distilled off
10. customThe residue obtained in this way
11. distillationwas distilled at 81-84° C./60 torr

ORD record

ord-8aee5449a9d54ce5b8cb59f427ec6f31

Source dataset

uspto-grants-2011_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07973114B2