## Abstract A simple one‐step syntheses of 2‐([^14^C]‐methyl) furan and 4‐oxo‐[5‐^14^C]‐2‐pentenal have been described. Carbon‐14 labeled 2‐methylfuran was synthesized by treatment of 2‐furyl lithium with ^14^C‐methyl iodide, and ^14^C‐acetylacrolein was obtained by peracid oxidation of labeled 2‐m
Synthesis of 1-pentene-4-14C and 1-pentene-5-14C
✍ Scribed by P. Ph. H. L. Otto; B. van Zanten
- Book ID
- 104586472
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 222 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
1‐Pentene‐4‐^14^C and 1‐pentene‐5‐^14^C were obtained in one single step from iodoethane‐1‐^14^C and iodoethane‐2‐^14^C, respectively, by reaction with allylmagnesium chloride in tetrahydrofurfuroxytetrahydropyran (TFTP) as solvent. The synthesis was carried out on a twenty mmoles scale in a completely closed apparatus. The pentenes were formed in 80 % yield. After final purification by means of gas‐liquid chromatography the radio‐chemical purity was 99.7 %.
📜 SIMILAR VOLUMES
## C1 c 1 (3) were formed together with (1). The NMR parameters of (l), its cis and trans isomers and (2) were obtained in C,D, solution at 100 MHz. Theoretical spectra of (1) at 60 MHz were simulated with the aid of a computer, using as input the NMR parameters obtained at 100 MHz and good agree