Reaktion #64789
ord-7d8e39d4020d4a3891cce6ef445e7172
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1FiltrationThe reaction mixture was then filtered into a flask
- 2Temperaturlet warm to -5° C.
- 3workup.STIRRINGstirred overnight
- 4SonstigeThe cold reaction mixture
- 5Filtrationwas then filtered
- 6Waschenthe filtrate was washed with water, saturated sodium bicarbonate, and brine
- 7TrocknenThe organic layer was dried (MgSO4)
- 8Filtrationfiltered
- 9Einengenconcentrated in vacuo
- 10Sonstigeto yield a reddish brown oil
- 11SonstigeThe oil was triturated with cold petroleum ether
- 12Sonstigeto yield 14.42 g
- 13EinengenThe mother liquors were concentrated
- 14Sonstigeto stand yielding a second crop of 1.96 g
Vorschrift
A solution of N-[[(1,1-dimethylethyl)oxy]carbonyl]-L-phenylalanine (20.01 g., 75 mmol) in 150 mL of dry tetrahydrofuran was chilled to -25° C. and treated with N-methylmorpholine (8.3 mL, 75 mmol) and isobutylchloroformate (9.8 mL, 75 mmol) and then stirred at -25° C. for 10 minutes. The reaction mixture was then filtered into a flask containing a solution of diazomethane (prepared from 35.48 g., 240 mmol of N-methyl-N'-nitro-N-nitrosoguanidine) in 300 mL of anhydrous ether at -78° C. and then let warm to -5° C. and stirred overnight. The cold reaction mixture was then filtered and the filtrate was washed with water, saturated sodium bicarbonate, and brine. The organic layer was dried (MgSO4), filtered and concentrated in vacuo to yield a reddish brown oil. The oil was triturated with cold petroleum ether to yield 14.42 g. of a light tan solid. The mother liquors were concentrated and allowed to stand yielding a second crop of 1.96 g. of light yellow crystals for a total yield of 16.38 g. of the title A compound as a tannish solid; m.p. 87°-90° C. [α]D =-32.2° (c=1.15, methanol).