Carbon Dioxide → HCID 86744639、化合物
反応式
[C:1](=[O:3])=O.Cl.[CH2:5]([O:7][C:8](=[O:12])[CH2:9][CH2:10][NH2:11])[CH3:6].C(N(CC)CC)C.P(Cl)(Cl)(Cl)=O>ClCCl.C(OCC)C>[N-:11]=[C:1]=[O:3].[CH2:5]([O:7][C:8](=[O:12])[CH2:9][CH2:10][NH2:11])[CH3:6][C:1](=[O:3])=O.Cl.[CH2:5]([O:7][C:8](=[O:12])[CH2:9][CH2:10][NH2:11])[CH3:6].C(N(CC)CC)C.P(Cl)(Cl)(Cl)=O>ClCCl.C(OCC)C>[N-:11]=[C:1]=[O:3].[CH2:5]([O:7][C:8](=[O:12])[CH2:9][CH2:10][NH2:11])[CH3:6]Carbon dioxide was added subsurface to a dichloromethane (40 mL) solution containing β-alanine ethyl ester hydrochloride salt (0.03 mol, 4.6 g), N-cyclohexyl-N',N',N",N"-tetraethylguanidine (0.03 mol, 7.6 g) and triethylamine (0.12 mol, 12.0 g) at -10° C. (ice and salt bath) for 40 min at a pressure of 0 psig. The reaction mixture was transferred rapidly via cannula under carbon dioxide to the precooled solution of phosphorus oxychloride (0.03 mol, 4.8 g) in 40 mL dichloromethane. After stirring for 20 min at -10° C. diethylether (50 mL) was added to the reaction mixture. A white ppt formed and was filtered off. The filtrate was concentrated in vacuo and the residue was extracted with 3×25 mL diethylether. The ether layers were concentrated and the residue was distilled under vacuum collecting product, β-alanine ethyl ester isocyanate, at 37°-39° C. (2.74 g, 64%) of 97.3% purity as judged by GC. IR (neat) 2272, 1732 cm-1. 1H NMR (CDCl3) δ 4.16 (q, 2H, J=4.3), 3.56 (t, 2H, J=6.4), 2.57 (t, 2H, J=6.4), 1.25 (t, 3H, J=7.2) ppm.
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