Abstract:CCDC no.: 1487250The asymmetric unit of the title structure is shown in the gure. Tables 1 and 2 contain details of the measurement method and a list of the atoms including atomic coordinates and displacement parameters.
Source of materialtert-Butyl 2-phenylethylcarbamate was synthesized from the reaction of 2-phenylethylamine with 1.2 equivalents of ditert-butyl dicarbonate in the presence of 1.5 equivalents of triethylamine in dichloromethane at 0°C for 15 minutes and
“…They can be synthesized using a variety of convenient processes (Blaser et al, 2012;Smith et al, 2012;Ibrahim et al, 2011;Porzelle et al, 2009;Lee et al, 2009;Lebel & Leogane, 2006;Caddick et al, 2003). The X-ray crystal structure of the related tert-butyl 2-phenylethylcarbamate was published recently (El-Hiti et al, 2016).…”
In the title molecule, C8H7BrClNO2, the bromochlorophenyl ring is inclined to the methylcarbamate unit by 32.73 (7)°. In the crystal, N—H...O hydrogen bonds form chains of molecules parallel to [100].
“…They can be synthesized using a variety of convenient processes (Blaser et al, 2012;Smith et al, 2012;Ibrahim et al, 2011;Porzelle et al, 2009;Lee et al, 2009;Lebel & Leogane, 2006;Caddick et al, 2003). The X-ray crystal structure of the related tert-butyl 2-phenylethylcarbamate was published recently (El-Hiti et al, 2016).…”
In the title molecule, C8H7BrClNO2, the bromochlorophenyl ring is inclined to the methylcarbamate unit by 32.73 (7)°. In the crystal, N—H...O hydrogen bonds form chains of molecules parallel to [100].
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