Thermal and photochemical reactions of a stable thiobenzaldehyde, 2,4,6-tri-t-butylthiobenzaldehyde
β Scribed by Renji Okazaki; Akihiko Ishii; Nobuo Fukuda; Hiroyuki Oyama; Naoki Inamoto
- Book ID
- 104232491
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 200 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Thermal and photochemical reactions of the title compound gave benzothiolane g in high yield; the reaction with free radicals also afforded 2 along with some other products.
We have recently reported the synthesisof the first stable thiobenzaldehyde, 2,4,6-tri-t-butylthiobenzaldehyde (L).' The ready availability and thermal stability of & enable us to study the chemical reactivities of the thioaldehyde about which only little has been known so far.
2 3 Recent papers on some reactions of thioaldehydes prompted us to report our preliminary results
π SIMILAR VOLUMES
The first rotational isomers of thiobenzaldehydes, TbtCH=S (2a and 2b: Tbt = 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl), were synthesized and isolated as stable crystalline compounds by the desulfurization of the corresponding overcrowded cyclic polysulfides TbtCHS, (n = 5 or 8) with phosphine rea