Synthesis of 2,3-bis(hydroxymethyl)-2,3-dinitro-1,4-butanediol tetrabenzoate (BHDBTB) with activa-tor of 4-dimethylaminopyridine (DMAP) and dehydrant of N,N-dicyclohexylcarbodiimide(DCC) has been carried out by esterification of 2,3-bis(hydroxymethyl)-2,3 dinitro-1,4-butanediol(BHDB) and benzoic acid. Structure of product was characterized by 1H NMR, 13C NMR and IR. The results of X-ray single-crystal diffraction show that BHDBTB belongs to triclinic system;the space group is P-1, Mr= 656.58. The crystal cell data of product were: a=8.851 nm,b=9.373 nm,c=10.211 nm,α=82.61°,β=83.31°,γ=67.74°,V=775.3 nm3,Z=2,Dc=1.406 g/cm3,R1=0.083 6,Rw2=0.086 1.%以2,3-二羟甲基-2,3-二硝基-1,4-丁二醇(BHDB)和苯甲酸为原料,4-二甲氨基吡啶(DMAP)为活化剂, N,N'-二环己基碳二亚胺(DCC)为脱水剂,通过酯化反应得到含能增塑剂2,3-二羟甲基-2,3-二硝基-1,4-丁二醇四苯甲酸酯(BHDBTB),对产物进行了1H NMR、13C NMR、IR等结构表征.X-射线单晶衍射说明,BHDBTB晶系属于三斜晶系,空间群为P-1,Mr = 656.58.晶体的数据为:a=8.851 nm,b=9.373 nm,c=10.211 nm,α=82.61°,β=83.31°,γ=67.74°,V= 775.3 nm3,Z=2,Dc=1.406 g/cm3,R1=0.0836,Rw2=0.0861.
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