摘要
以β-萘乙烯为原料,通过烯烃的Sharpless不对称双羟化、环化、开环、催化氢化、甲酰化、还原等6步反应,生成标题化合物,总产率以β-萘乙烯计为39.7%,e.e.值高达97%-99%。对产物进行了质谱、红外光谱、^1HNMR和^13CNMR表征。
( S )-( + )-2-( 2-Naphthyl )-2-( N-methyl ) aminoethanol was synthesized from ( R )-1-naphthalen-2- ylethane-1,2-diol produced by the Sharpless asymmetric dihydroxylation, eyelization of diols, azide opening of epoxides, catalytic hydrogenation of the resulting azido alcohols, formylation of the chiral β-amino alcohol and reduction of the corresponding formamide. The six-step procedure starting from 2-vinylnaphthalene resulted in a total yield of 39.7% with the e. e.values reaching up to 97% - 99%. Its structure was characterized by IR, ^1HNMR, ^13CNMR and MS.
出处
《化学试剂》
CAS
CSCD
北大核心
2007年第3期132-134,共3页
Chemical Reagents
基金
国家自然科学基金资助项目(20372083)