[11C]Methylenetriphenylphosphorane, a new 11C-precursor, used in a one-pot wittig synthesis of [β-11C]styrene
✍ Scribed by Tor Kihlberg; Per Gullberg; Bengt Långström
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- French
- Weight
- 299 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Preparation of [^11^C]methyltriphenylphosphonium iodide and the in situ generation of [^11^C]methylenetriphenylphosphorane directly from [^11^C]methyl iodide, is described. Using this one‐pot preparation, [β‐^11^C]styrene was synthesized conveniently, fast and with a minimum of manual handling. The synthesis was performed by using [^11^C]methyl iodide, triphenylphosphine, epichlorohydrin and benzaldehyde in tetrahydrofurane/o‐dibromobenzene, with a synthesis time of 40 min (counted from the end of [^11^C]methyl iodide transfer), a radiochemical yield of 80–90% of [β‐^11^C]styrene and a specific radioactivity, of 100MBq/μmol. In a typical experiment starting with 960 MBq ^11^C‐methyl iodide, 200 MBq of [β‐^11^C]styrene was obtained within 42 min.
📜 SIMILAR VOLUMES
N a t i o n a l Laboratory, Upton, NY 11973 Received Sumary A r a p i d , one-pot, s y n t h e s i s of cyclopropane [ llC]carbonyl c h l o r i d e was developed. This s y n t h e s i s proceeded i n 807; r a d i ochemical y i e l d (EOB) i n a s y n t h e s i s time of LO minutes. This a c i d c h
## Abstract 2β‐Carbomethoxy‐3β‐(4‐fluorophenyl)‐[N‐^11^C‐methyl]tropane, a potent inhibitor of dopamine transport, was prepared by N‐methylation of the appropriate nor‐methyl precursor in DMF with [^11^C]iodomethane. After derivatization of unreacted precursor with a long chain acyl halide, the rad
## Abstract A new approach for ^11^C–C bond formation via a Sonogashira‐like cross‐coupling reaction of terminal alkynes with [^11^C]methyl iodide was exemplified by the synthesis of 17__α__‐(3′‐[^11^C]prop‐1‐yn‐1‐yl)‐3‐methoxy‐3,17__β__‐estradiol. The LC‐purified title compound was obtained in dec
## Abstract [__N__‐Methyl‐^11^C]choline has been synthesized at room temperature by the reaction of [^11^C]CH~3~I with 2‐dimethylaminoethanol (DMAE), with the latter directly loaded on a weak cation‐exchange cartridge. Most of the efforts have been directed to reduce the amount of residual precurso