Benzyl chloroformate → Benzyl 3-pyrroline-1-carboxylate
Reaktionsgleichung
[CH2:1]([O:8][C:9](Cl)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([N:19]1[CH2:23][CH:22]=[CH:21][CH2:20]1)C1C=CC=CC=1>ClCCl>[CH2:1]([O:8][C:9]([N:19]1[CH2:23][CH:22]=[CH:21][CH2:20]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
43 mL benzyloxycarbonyl chloride in 135 mL dichlormethane was added to 17.6 g 1-benzyl-2,5-dihydro-1H-pyrrole in 135 mL dichlormethane at 0° C. in 60 min. The mixture was stirred 3 h at RT and washed with saturated sodium hydrogencarbonate solution. The organic layer was dried and evaporated. The residue was purified by chromatography on silica gel (hexane/ethyl acetate: 5/1) to give 19.7 g of the desired product.
Aufarbeitung
- washwashed with saturated sodium hydrogencarbonate solution
- customThe organic layer was dried
- customevaporated
- customThe residue was purified by chromatography on silica gel (hexane/ethyl acetate: 5/1)
Quellen und Nachweise
- ORD-Eintrag
- ord-9046dd2206b54659ba959159c5c333c1
- Quelldatensatz
- uspto-grants-2014_06
- Patentnummer
- US08741892B2
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