Preparation of Dialkyl 1-(Alkylamino)alkylphosphonates, Alkyl [1-(Alkylamino)alkyl]phenylphosphinates and [1-(Alkylamino)alkyl]diphenylphosphine Oxides via 'In Situ' Generated Iminium Ions

被引:7
|
作者
Goldeman, Waldemar [1 ]
Soroka, Miroslaw [1 ]
机构
[1] Wroclaw Univ Technol, Dept Chem, PL-50370 Wroclaw, Poland
来源
SYNTHESIS-STUTTGART | 2010年 / 14期
关键词
aminophosphonates; aminophosphinates; imines; Schiff bases; nucleophilic addition; PYRIDINE AMINOPHOSPHINE OXIDES; SCHIFF-BASES; DIPHENYLPHOSPHINE OXIDE; PHOSPHORUS-COMPOUNDS; ASYMMETRIC-SYNTHESIS; ACIDS; ESTERS; BOND; PHOSPHITE; CLEAVAGE;
D O I
10.1055/s-0029-1218817
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The reaction of trialkyl phosphites, dialkyl phenylphosphonites or alkyl diphenylphosphinites with N-alkylalkanimines in the presence of hydrogen chloride gives dialkyl 1-(alkylamino) alkylphosphonates, alkyl [1-(alkylamino)alkyl]phenylphosphinates or [1-(alkylamino) alkyl] diphenylphosphine oxides respectively, via Arbusov-like reaction of iminium salts generated 'in situ' from N-alkylalkanimines. This reaction is an alternative and competitive to known method of preparation based on the addition of H-P compounds to N-alkylalkanimines, because it gives higher yields, no heating is necessary, and the isolation of products is easy.
引用
收藏
页码:2437 / 2445
页数:9
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