Boc-L-alanine methyl ester → tert-butyl N-((2S)-1-oxopropan-2-yl)carbamate

Boc-L-alanine methyl ester (5.0 g, 24.6 mmol) was dissolved in dry toluene (150 ml) under an argon atmosphereand cooled in a dry ice-acetone bath. To this vigorously stirred solution was added a solution of diisobutylaluminumhydride (1.0M in hexanes, 61.5 ml, 61.5 mmol), pre-cooled in a dry ice-acetone bath, via a transfer needle. After 6 minutes, the reaction was carefully quenched with methanol (4 ml) and the mixture allowed to warm to room temperature. The reaction mixture was poured into a separatory funnel containing 250 ml ether and 200 ml of ice cold 0.25N hydrochloric acid. The layers were separated and the organic layer was washed with 0.25N hydrochloric acid (3×80 ml) and brine (50 ml). The organic layer was dried overmagnesium sulfate, filtered and concentrated using a rotary evaporator at ambient temperature. The residue was chromatographed using hexanes--30% ethylacetate to give Boc-L-alaninal. The compound may also be prepared by the technique described in Synthesis, 1983, pg. 676.

1. temperaturecooled in a dry ice-acetone bath
2. temperaturepre-cooled in a dry ice-acetone bath, via a transfer needle
3. customthe reaction was carefully quenched with methanol (4 ml)
4. additionThe reaction mixture was poured into a separatory funnel
5. additioncontaining 250 ml ether and 200 ml of ice cold 0.25N hydrochloric acid
6. customThe layers were separated
7. washthe organic layer was washed with 0.25N hydrochloric acid (3×80 ml) and brine (50 ml)
8. dry with materialThe organic layer was dried overmagnesium sulfate
9. filtrationfiltered
10. concentrationconcentrated
11. customa rotary evaporator at ambient temperature
12. customThe residue was chromatographed

ORD record

ord-af6ae102f92746acb75008a478eaa29e

Source dataset

uspto-grants-1996_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05496927