Observations on the vilsmeier reaction part 1
✍ Scribed by Andrew P. Shawcross; Stephen P. Stanforth
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 606 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
Rre reaction of N~~i~tit~t~~~yl~i~~~ derivatives under Vilsmeie~&ditions afforded proikt~ derived from an intramlecular hydride shift when one ,N=substituent was benzyl or 4-chlurobenzyf. introduction of a forz@l group into electron-rich arcmtic systems. W have investigated the Vilsmeier reaction of N,N_dis~tituted_6~~iline derivatives tltf-(3) and, for ccqmrison, &N_dSsubstitu;ed aniline derivatives (4) and (S), Preparatia of ccarpcKprds (l)-f5) N,~~(2~~yl)-4-~thylaniline fl) was prepared by cYano&hylation of -_I 4-mthylaniline4. CXqomds ~2bW were all prepared by a simi.lar qanoethylation pmcedue. plus, _Wyl-4inethyUniline afforded !!!-~~~f2~ Yl)-e-=thylaniline ((2) (46% yield), 1461
📜 SIMILAR VOLUMES
## Abstract 5‐Imino‐3‐methyl‐l‐phenyl‐2‐pyrazoline‐4‐dithiocarbamic acid (I) underwent simultaneous formylation and dimerization reactions with the Vilsmeier reagent giving 4‐[5′‐imino‐3‐(1″‐formyl‐2″‐dimethylaminoethenyl)‐3′‐methyl‐1′‐phenyl‐1′H‐pyrazolo‐4′‐dithiocarbamyl‐2,4‐dihydro‐3‐imino‐5‐met