Preparation of β -alanine-3,3-D2 and −2,2,3,3-D4
✍ Scribed by Kazuhiko Hanai; Akio Kuwae
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- French
- Weight
- 263 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
B -Alanine-3,3-d2 and -2,2,3,3-d4 were prepared via a five-step procedure from ethyl cyanoacetate. The procedure involves reduction of the starting material with lithium aluminum deuteride, followed by benzoylation of the amino alcohol obtained, oxidation of the benzoylated compound, hydrolysis of benzoyCB -alanine-3,3-d2 with hydrochloric or deuterochloric acid, and then anion exchange of the hydrochloride or the deuterochloride.
The isotopic purities of the d2 and d4 compounds were more than 98 and 97%. respectively.
📜 SIMILAR VOLUMES
S p e c i f i c a l l y l a b e l e d , o p t i c a l isomers of a l a n i n e were synthesized from acetic-13C2 a c i d by a six-tjtep procedure with y i e l d s of 37-38% of t h e o p t i c a l l y a c t i v e m a t e r i a l .
In connection with our microwave investigations of phenol, all the monodeuteriophenols with deuterium at the ring atoms were prepared, and their purity established by PMR and IR-spectroscopy. 2-D, 3-D AND 4-D-PHENOL.