this catapeon 
-Also the occurrence of Hie hypothetical ammonium group er 
| easy disintegration of the structure into single molecules. _ a é 
5 oe As by-product in the preparation of aldehyde-ammonia, according | ie the Ider 
-- method known, a new compound was obtained — dihydroxytriethylidenediimine, a} 
‘to 47°, which represents: a condensation produ er of the pinolecua aldehyde amr 
with aldehyde. . ati it : Perec yas 400; 
eee EON Ge CH: one ae 
: HN ‘NH ) ie OH en 
eae Wee CH, CHC od 
ap CH;-HC CH-CHs NA; - OH © 
ies SO | -CH;-CH oa ee 
Bie a7 7 NH | ‘NH: vig we 
(I) 2,4, 6-Trimethylhexahydro-1, 3, 5-triazine : ~ (11) Common trimolecular aldehyde-ammonia 
(aldehyde-ammonia after Delépine). after Aschan, . Pi iam 
» < Re action of benzyl alcohol, benzaldeh yde and benzyl ester on ‘helminthes see 
x 
of this Report. 
Ketones. 
_ from ibtayiaheivibeiane, uaa octyl Alcohol’ 
-nonylcarbinol, and from acetophenone, methyiphenylearbinol ‘Whilst aldehy y 
_ kingdom as intermediate links in tinction: fe eiahplie processes, apie is 
et eee acid excepted — pele the fact. that Bee are. he) 
j ; 1 ie 
1) Compt. renit, 128 (1899), 105. a a Ct. Be Te 140. A y Berl. Bor 
