Methyl trifluoromethyl ketone → HCID 57786809, compound

Temperature

-78 °C

To a solution of prop-2-ynyl-carbamic acid tert-butyl ester (0.646 g, 4.16 mmol) in 15 mL of tetrahydrofuran at −78° C. was added lithium diisopropylamide (2.0 M solution in heptane/THF/EtPh, 4.6 mL, 9.2 mmol) all at once. The orange solution was stirred at −78° C. for 2 h, at which point it is a cloudy yellow mixture. 1,1,1-Trifluoroacetone (0.5 mL, 5 mmol) was added all at once, and the yellow mixture was stirred, allowing to slowly warm to RT, for 17.5 h. A sat. aq. NH4Cl solution (30 mL) was added, and the mixture was extracted with 30 mL of ether. The organic layer was sequentially washed with 30 mL of water and 30 mL of a sat. aq. NaCl solution, dried over MgSO4, filtered and concentrated to an orange cloudy oil. Column chromatography (20->40% EtOAc/hexanes) afforded 0.687 g (62%) of slightly impure (5,5,5-trifluoro-4-hydroxy-4-methyl-pent-2-ynyl)-carbamic acid tert-butyl ester as a yellow oil that was used without further purification.

1. stirringwas stirred
2. temperatureto slowly warm to RT, for 17.5 h
3. extractionthe mixture was extracted with 30 mL of ether
4. washThe organic layer was sequentially washed with 30 mL of water and 30 mL of a sat. aq. NaCl solution
5. dry with materialdried over MgSO4
6. filtrationfiltered
7. concentrationconcentrated to an orange cloudy oil

ORD record

ord-b17facdfae074adea58ba72224fcd74d

Source dataset

uspto-grants-2013_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08426441B2