Abstract

1. It has been established that by the decarboxylation of the glycidic acid , obtained by Darzens' method from cis-decahydro-2-naphthol of m.p. 105°, a mixture of stereoisomeric decahydro-2-naphthaldehydes is formed; these have not been investigated further. 2. The synthesis has been affected, by Rodionov's method, of β-(2-decalyl)-β-alanine (β-aminodecahydro-2-naphthalenepropionic acid), which also appeared to be a mixture of isomers, the separation of which was not carried out. 3. By taking advantage of the different ether-solubilities of the acid chlorides of the N-benzoylated β-(2-decalyl)-β-alanines, the corresponding amides, m.p. 210–212° and 250–252°, were isolated. 4. The two amides were converted by careful hydrolysis into the isomeric N-benzoylated β-(2-decalyl)-β-alanines. 5. It has been shown that when the amide of N-benzoyl-β-(2-decalyl)-β-alanine is heated with acetic anhydride, a transacylation reaction occurs, and instead of 6-(2-decalyl)-6,6-dihydro-2-phenyl-4(3H)-pyrimidinone the corresponding 2-methyl derivative is obtained. 6. In order to characterize β-(2-decaclyl)-β-alanine, the corresponding ureido acid and 6-(2-decalyl)-hydrouracil were prepared. 7. Esters and hydrazides of N-benzoyl-β-(2-decalyl)-β-alanine have been prepared, and, by means of the Curtius reaction, they have been converted into 3-benzoyl-4-(2-decalyl)-2-imidazolidones and the corresponding 4-(2-decalyl)-2-imidazolidinone.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call