杏耀代理1980

乙炔酯对环烯胺进行，接着重排扩环，得到多两个碳的环二烯胺的。产物水解后可以得到多两个碳的环二烯酮。

反应机理

反应操作

1-(N-Morolino)-2,3-dicarbomethoxy-1,3-cycloheptadiene (4). DMAD 1 (16.2 g, 77.4 mmol) was added to morpholinocyclopentene 2 (11 g, 77.4 mmol) in PhH (40 mL) under N2 with ice cooling and stirring at su a rate that the temp never rose above 50 C. After a short supplementary stirring, the mixture was heated to reflux for 12 h. The solution was treated with excess Et2O under cooling and the precipitate was filtered off. Recrystallization from Me2CO afforded 11.4 g of 4 in 48% yield, mp 167–168 C.

2,3-Dicarbomethoxy-3-cycloheptenone (5).  A solution of 4 (1 g, 3.25 mmol) in MeOH (5 mL) and 32% HCl (1 mL) was heated to reflux. Water (2 mL) was added and the mixture was heated for another 10 min to reflux. After cooling, the precipitate was crystallized from MeOH:H2O 2:1 to give 610.5 mg of 5 in 90% yield, mp 63.5–64 C.

【Berchtold GA, J Org Chem, 1963, 28, 1459】

相关文献

1 Brannock KC J Org Chem 1961 26 625

2 Berchtold GA J Org Chem 1961 26 3043

3 Berchtold GA J Org Chem 1963 28 1459

4 Hickmott PW Tetrahedron 1982 38 3363

5 Mark J Tetrahedron 2000 56 4317

6 Miesch M J Org Chem 2003 68 433

编译自：Organic Syntheses Based On Name Reactions, 3RdEd, A. Hassner, Page 41.

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