Synthesis of [1-14C-carboxy]-4-benzoylbenzoic acid
✍ Scribed by Kay L. Nakamaye; Ralph G. Yount
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- French
- Weight
- 266 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
1-14C-Ca oxy]-4-benzoylbenzoic acid has been prepared v i a a Grignard r e a c t i o n w i t h %Oz.
4-Bromobenzophenone was converted t o (4-braopheny1)phenyldichloranethane using phosphorus pentachloride. was reacted w i t h methoxide i o n t o form 4-bromobenzophenone dimethyl k e t a l which was subsequently converted t o i t s Gsignard reagent, carboxylated with 14CO2, and acid hydrolyzed t o t h e f i n a l product. reagent, v i r t u a l l y q u a n t i t a t i v e conversion of 14C02 t o product was obtained.
The d i c h l o r o canpound
Using excess Grignard
📜 SIMILAR VOLUMES
## Abstract A modification of the Sandmeyer reaction which requires only a moderate excess of cyanide‐^14^C was utilized for the preparation of 4‐chloro‐2‐fluorobenzonitrile‐7‐^14^C (3). After hydrolysis, the resulting acid (4) was converted to carboxy labelled furosemide (6) by existing methods. T
## Abstract The syntheses of [γ‐^14^C]‐γ‐oxo‐2‐dibenzofuranbutanoic acid (furobufen) 7 and 2‐dibenzofuranacetic[carboxy‐^14^C] acid 3b, a major metabolite of furobufen, are described. A by‐product, the dialkylated malonate 6 obtained in the synthesis of 7, was isolated and characterized.
Specifically labelled phenylacetic acid and mandelic acid derivatives, metabolites of L-Dopa, have been synthesized via the intermediary labelled benzyl alcohols, which were prepared by reduction of the methyl esters of the appropriate benzoic acids. The benzyl alcohols have been converted to the co
## Abstract The title work proceeds in five steps and 16% overall yield from sodium [1‐^14^C]acetate, which was converted by bromination followed by ethoxide displacement and reaction with phthaloyl dichloride to ethoxy[1‐^14^C]acetyl chloride. The thermal[2+2]cycloaddition of tetraethoxyethene wit