摘要
At 200 ℃ and 50 mPa, the oxidative carbonylation of amines catalyzed by organic gold complexes HAuCl 4, Au(PPh 3)Cl, Au(PPh 3) 2Cl, Au(PPh 3)NO 3 and [Au(PPh 3)] 2S afforded R(NHCO 2CH 3) n with a high conversion and selectivity. The best results were obtained when using the catalyst Au(PPh 3)Cl in the presence of PPh 3. The catalytic efficiency of catalytic Au(PPh 3)Cl was compared to Pd(PPh 3) 2Cl 2, e.g. the conversion was 97.2% and selectivity was 89% when using catalyst Au(PPh 3)Cl in the presence of PPh 3, while the conversion was 98.8% and selectivity was 86% when using catalyst Pd(PPh 3) 2Cl 2 in the presence of PPh 3. The experimental results suggested that Au complexes might be promising catalysts instead of Pd catalysts for the oxidative carbonylation of amines to carbamates.
At 200 ℃ and 50 mPa, the oxidative carbonylation of amines catalyzed by organic gold complexes HAuCl 4, Au(PPh 3)Cl, Au(PPh 3) 2Cl, Au(PPh 3)NO 3 and [Au(PPh 3)] 2S afforded R(NHCO 2CH 3) n with a high conversion and selectivity. The best results were obtained when using the catalyst Au(PPh 3)Cl in the presence of PPh 3. The catalytic efficiency of catalytic Au(PPh 3)Cl was compared to Pd(PPh 3) 2Cl 2, e.g. the conversion was 97.2% and selectivity was 89% when using catalyst Au(PPh 3)Cl in the presence of PPh 3, while the conversion was 98.8% and selectivity was 86% when using catalyst Pd(PPh 3) 2Cl 2 in the presence of PPh 3. The experimental results suggested that Au complexes might be promising catalysts instead of Pd catalysts for the oxidative carbonylation of amines to carbamates.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2001年第4期645-647,共3页
Chemical Journal of Chinese Universities
基金
中国科学院知识创新
甘肃省经济贸易委员会重点技术创新支持项目! (批准号 :1999-5 49)资助
