In 2017,Beilstein Journal of Organic Chemistry included an article by Liu, Xinyun; Phan, Johnny H.; Haugeberg, Benjamin J.; Londhe, Shrikant S.; Clift, Michael D.. Synthetic Route of C9H13NO. The article was titled 《Quinone-catalyzed oxidative deformylation: synthesis of imines from amino alcohols》. The information in the text is summarized as follows:
A new method for imine synthesis by way of quinone-catalyzed oxidative deformylation of 1,2-amino alcs. is reported. A wide range of readily accessible amino alcs. and primary amines can be reacted to provide N-protected imine products. The methodol. presented provides a novel organocatalytic approach for imine synthesis and demonstrates the synthetic versatility of quinone-catalyzed oxidative C-C bond cleavage. The results came from multiple reactions, including the reaction of 2-Amino-2-(4-methylphenyl)ethan-1-ol(cas: 157142-48-8Synthetic Route of C9H13NO)
2-Amino-2-(4-methylphenyl)ethan-1-ol(cas: 157142-48-8) belongs to anime. The reaction of alkyl halides, R―X, where X is a halogen, or analogous reagents with ammonia (or amines) is useful with certain compounds. Not all alkyl halides are effective reagents; the reaction is sluggish with secondary alkyl groups and fails with tertiary ones. Its usefulness is largely confined to primary alkyl halides (those having two hydrogen atoms on the reacting site).Synthetic Route of C9H13NO
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts