Sodium Hydroxide → HCID 70539013, compound
Reaction equation
COC([N:5]1[N:12](C(OC)=O)[CH:11]2[CH:6]1[CH:7]1[CH:17]([O:18]C(=O)C)[CH:10]2[CH:9]=[CH:8]1)=O.[OH-].[Na+].[O-]Cl.[Na+]>>[OH:18][CH:17]1[CH:10]2[CH:9]=[CH:8][CH:7]1[CH:6]1[CH:11]2[N:12]=[N:5]1Participants
4
Procedure
92 parts of 3,4-dimethoxycarbonyl-9-acetoxy-3,4-diazatricyclo[4,2,1,02,5 ]non-7-ene and 570 parts of 20 percent strength aqueous NaOH were stirred for 3 hours at 70° C., after which 356 parts of 13 percent strength by weight aqueous NaOCl were added dropwise at 40° C. and stirring was continued for 1 hour at 40° C. The reaction mixture was extracted continuously for 12 hours with 300 parts of CH2Cl2, the organic phase was dried with MgSO4, treated with active charcoal and evaporated down, and the residue was digested with 200 parts of petroleum ether. 36.4 parts (86 mol %) of 9-hydroxy-3,4-diazatricyclo[4,2,1,02,5 ]nona-3,7-diene of melting point 128° C. (from cyclohexane) were obtained. ##STR13##