Ethyl bromoacetate → Glycine, N-cyclopropyl-, ethyl ester
Reaktionsgleichung
[CH:1]1([NH2:4])[CH2:3][CH2:2]1.Br[CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8]>C(Cl)Cl>[CH2:10]([O:9][C:7](=[O:8])[CH2:6][NH:4][CH:1]1[CH2:3][CH2:2]1)[CH3:11]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Cyclopropylamine (12.1 mL, 175 mmol) and TEA (42 mL, 385 mmol) were combined at 0° C. in 350 mL CH2Cl2, then ethyl bromoacetate (19.4 mL, 175 mmol) was added dropwise. The reaction was warmed to RT for 3 h, then diluted with additional CH2Cl2, washed with water, sat. NaHCO3, and brine, dried (Na2SO4), filtered and concentrated. Flash filtration (silica, 30% EtOAc/hexane) provided 7-2 as a light yellow oil.
Aufarbeitung
- washwashed with water, sat. NaHCO3, and brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- filtrationFlash filtration (silica, 30% EtOAc/hexane)
Quellen und Nachweise
- ORD-Eintrag
- ord-be7779995e93436b865703de933e95b0
- Quelldatensatz
- uspto-grants-1999_09
- Patentnummer
- US05952306
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