## Abstract The title work proceeds in five steps and 16% overall yield from sodium [1β^14^C]acetate, which was converted by bromination followed by ethoxide displacement and reaction with phthaloyl dichloride to ethoxy[1β^14^C]acetyl chloride. The thermal[2+2]cycloaddition of tetraethoxyethene wit
Synthesis of [18-14C]octatriacontane from [1-14C]stearic acid
β Scribed by Saifunnissa B. Hassam
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- French
- Weight
- 490 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
β¦ Synopsis
14
A method was developed to synthesize C-labelled n-qtkanes for use in cigarette smoke studies. Specifica],ly, n-[18-Cloctatriacontane was synthesized from 1 mCi [l-Clstearic acid in a radiochemical yield of 20%. synthesis were two consecutive alkylations yf tosylmethyl isocyanide followed by acid hydrolysis to [18-Cl-19-octatriacontanone and modified Wolff-Kishner reduction tolfhe n-alkane. After purification on silica gel 25 mg of 118-Cloctatriacontane was obtained with a total radioactivity of 200 uC1, a specific activity o f 4.3 mCi/mmol, and a radiochemical purity in excess of 98% by thin layer radiochromatography. The method has also been applied to the synthesis of unlabeled n-pentatriacontane and is considered to be generally applicable to the synthesis of radiolabeled alkanes from radiolabeled fatty acids.
[ 18-4C I octatri acontane, radiosynthesi s, C-1 abeled a1 kanes.
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