反应详情

Diethyl 2-aminononanedioate (5.0 g) was heated with benzaldehyde (2.15 g) in benzene (10 ml) under reflux for 12/3 hours, removing the water formed by means of a Dean and Stark apparatus. The benzene was evaporated in vacuo and the residual oil was taken up in dry tetrahydrofuran (20 ml), stirred under dry nitrogen, treated with sodium hydride (0.61 g of a 80% dispersion in mineral oil), and heated until evolution of hydrogen began. Thereafter, reaction was allowed to proceed at room temperature. When effervescence had ceased, the pale yellow-brown solution was cooled in icewater and, with continued stirring, treated with methyl iodide (6.83 g); the cooling bath was removed after 15 minutes and the mixture was set aside at room temperature overnight. The resulting suspension of solid ws diluted with ether (100 ml) and skaken with ice-cold water (100 ml), and the ethereal phase was washed with H2O, dried over sodium sulphate, and evaporated, to leave crude diethyl 2-(benzylideneamino)-2-methylnonanedioate (6.4 g) as a yellow oil.

1. temperatureunder reflux for 12/3 hours
2. customremoving the water
3. customformed by means of a Dean and Stark apparatus
4. customThe benzene was evaporated in vacuo
5. additiontreated with sodium hydride (0.61 g of a 80% dispersion in mineral oil), and
6. temperatureheated until evolution of hydrogen
7. customThereafter, reaction
8. customto proceed at room temperature
9. temperaturethe pale yellow-brown solution was cooled in icewater and, with continued stirring
10. customthe cooling bath was removed after 15 minutes
11. additionThe resulting suspension of solid ws
12. additiondiluted with ether (100 ml)
13. washthe ethereal phase was washed with H2O
14. dry with materialdried over sodium sulphate
15. customevaporated