Preparation of sodium 2-mercapto-[14C]ethanesulfonate
✍ Scribed by J. Jarý; V. Grossmann; S. Doležal; J. Labsk´
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 190 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Starting from C1-14Cl ethanol 1 , 2-dibrom-C14C1ethane was prepared by an usual method through C14C3ethylene. Sodium sulfite was alkylated by 1,2-dibrom--C Clethane and the formed sodium 2-br0m-L~~Clethane sulfonate was transferred without isolation to a labelled 2-I: (aminoiminomethyl) thiol -C14C1 ethanesulfonic acid. After purification by crystallization of the acid 2-mercapto-C14C1 ethanesulfonic acid was prepared through guanidinium salt. After the neutralization of 2-mercapto-[l4C1 ethanesulfonic acid by sodium hydroxide the corresponding sodium salt with specific activity 0.083 pCi/mmol ( 0 . 3 1 MBq/mmol) was prepared.
📜 SIMILAR VOLUMES
## Abstract [^14^C]Methane (440 mCi) was prepared using the reduction of [^14^C]methyl iodide by sodium borohydride in diglyme in quantitative yield. The diborane formed was trapped as nonvolatile 9‐BBN. [^14^C]Methane free of any accompanying gases was conveniently distributed into calibrated glas
## Abstract ^14^C~2~‐Pentaerythritol (^14^C‐PE) at approximately 8 mCi/mmole was prepared in 76% yield on a 3‐mmole scale via a base‐catalyzed condensation of acetaldehyde‐^14^C~2~ with 1.5% aqueous CH~2~O.
A high-yield, relatively simple synthetic route leading to incorporation of l'C into the secondary position of the adamantane nucleus is described. The synthesis was achieved by the sequence shown in Figure 2. The key steps involved the introduction of a I4C label by diazome1hane-14C ring expansion
## Abstract Chloral‐1,2‐^14^C hydrate was prepared by direct chlorination of labeled acetaldehyde in an overall 47% radiochemical yield. The reaction was carried out without a catalyst by heating at one temperature in a single stage reaction. No lower chloroacetaldehydes were detected.