Name | 2-TERT-BUTYL-1,3-DIISOPROPYLISOUREA |
Synonyms | 2-TERT-BUTYL-1,3-DIISOPROPYLISOUREA O-tert-Butyl-N,N'-diisopropylisourea tert-Butyl N,N'-diisopropylcarbaMiMidate tert-Butyl N,N'-diisopropylimidocarbamate tert-butyl N,N'-bis(1-methylethyl)imidocarbamate CarbaMiMidic acid, N,N'-bis(1-Methylethyl)-, 1,1-diMethylethyl ester |
CAS | 71432-55-8 |
Molecular Formula | C11H24N2O |
Molar Mass | 200.32 |
Density | 0.89±0.1 g/cm3(Predicted) |
Boling Point | 61°C/10mmHg(lit.) |
pKa | 9.54±0.50(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
Refractive Index | 1.4240-1.4280 |
Use | Uses O-tert-butyl-N,N'-diisopropylisourea is a useful synthetic intermediate for the synthesis of 5-Oxo atorvastatin tert-butyl ester, which is a Boc-protected derivative of atorvastatin. O-tert-butyl-N,N'-diisopropylisourea is also used as a total synthetic reagent for the antifungal natural product sitrafengin A. |
Raw Materials | tert-Butanol N,N'-Diisopropylcarbodiimide |
Downstream Products | N-1-Boc-amino-3-cyclopentene 2-TERT-BUTYL-1,3-DIISOPROPYLISOUREA |
at room temperature, the mixture of DIC(2.52 g1.0eq.) and tert-butanol (1.8 g1.2eq.) is placed in a round-bottomed flask and a catalytic amount of CuCl is added, and then the reaction system is replaced by N2 protection. Stir for 4 days to obtain the crude dark green compound as described in the title, which is directly used for the next reaction.