Preparation of n-butoxy(13C2-acetic) acid, 1-n-butoxy-2-hydroxy (13C2-ethane), (n-butoxy-2′,2′,3′,3′,4′,4′,4′-d7)acetic acid, and 2-(n-butoxy-2′,2′,3′,3′,4′,4′,4′-d7)ethanol
✍ Scribed by James R. Pribish
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 401 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
(n‐Butoxy‐2′,2′,3′,3′,4′,4′,4′‐d~7~)acetic acid (1) and 2‐(n‐butoxy‐2′,2′,3′,3′,4′,4′,4′‐d~7~)ethanol (2) have been prepared in high yield from n‐butanol‐2,2,3,3,4,4,4‐d~7~. n‐ Butoxy(^13^C~2~‐acetic) acid (3) and 1‐n‐butoxy‐2‐hydroxy(^13^C~2~‐ethane) (4) have also been synthesized using bromoacetic‐^13^C~2~ acid as the source of labelled carbon. The main complication in the development of the process was partial conversion of butoxyacetic acid to butyl butoxyacetate during GC analysis, which hampered evaluation of trial reactions.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
HCl) was synthesized through a straightforward six-step sequence from the readily available [ 14 C-carbonyl]methyl salicylate (2). The overall radiochemical yield of the 1 . 2 HCl from 2 was 10.5%, and its radiochemical purity was 98.8%.