SYNTHESIS OF DI-TERT-BUTYL METHYLENEMALONATE, A STERICALLY HINDERED 1,1-DICARBONYL ALKENE

SYNTHESIS OF DI-TERT-BUTYL METHYLENEMALONATE, A STERICALLY HINDERED 1,1-DICARBONYL ALKENE
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DOI:
10.1021/jo00168a061
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发表时间:
1983-01-01
影响因子:
3.6
通讯作者:
WONG, J
WONG, J
中科院分区:
化学2区
文献类型:
--
作者:
BALLESTEROS, P;ROBERTS, BW;WONG, J

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NMR spectroscopic analysis of 5 obtained in this fashion indicated the presence of small amounts of starting ester 1 and bis (hydroxymethyl) derivative 8 (vide infra) as contaminants. The latter was removed by a second distillation to give an overall yield of 53% of 5 containing a trace of 1. In our experience, the presence of 1 has presented no interference to reactions of 5, and there has been no necessity for further purification. 5 was obtained as a mobile, clear liquid, the stability of which contrasts sharply with that of simpler methylene-malonate esters. Thus freshly prepared samples have been kept at room temperature for up to 4 weeks with no observable change as indicated by XH NMR spectroscopy. Infrequently, however, some samples have developed a