Reaction #1312049
Related Literature (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US06737429B2
Conditions: temp:2.51; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of 10.9 g of N-tert.-butoxycarbonylglycine N-methyl-N-methoxyamide in 300 ml of anhydrous tetrahydrofuran and 100 ml of anhydrous diethyl ether was cooled at 0-5° C. while 100 ml of a 2M solution of isopropyl magnesium chloride in tetrahydrofuran was added slowly. The mixture was stirred at 0-5° C. for 4 h then poured into 1.5 liter of 1M hydrochloric acid. The product was extracted with three portions of 500 ml diethyl ether. Combined extracts were washed with 500 ml brine then dried over anhydrous magnesium sulphate, filtered and evaporated to give 8.38 g of 4-tert.-butoxycarbonylamino-2-methyl-3-butanone as a colourless oil which was used without further purification. was added slowly The product was extracted with three portions of 500 ml diethyl ether Combined extracts were washed with 500 ml brine then dried over anhydrous magnesium sulphate filtered evaporated
Source ID: ord-a619453196f548b0bd8d2c626b8e690d