Selective synthesis of some 5-hydrazono-5,6,7,8-tetrahydro-2H-1-benzopyran-2-ones
✍ Scribed by Polonca Trebše; Boris Recelj; Marijan Kočevar; Slovenko Polanc
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 320 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
A simple, highly selective transformation of 5,6,7,8‐tetrahydro‐2__H__‐1‐benzopyran‐2,5‐diones 1–3 and 14 with some phenylhydrazines and heterocyclic hydrazines to 5‐hydrazono‐2__H__‐1‐benzopyran‐2‐ones 4–12 and 15–16 is described. Under more severe conditions the hydrazonoquinoline derivative 17 was obtained from the benzopyran derivative 3 and Phenylhydrazine.
📜 SIMILAR VOLUMES
I211 Genbve 4 (5. V .86) ~ Comparative results on the reduction of 4,6,7,8-tetrahydro-7,7-dimethyl-2H-1 -benzopyran-2,5(3H)-diones 1 are reported. Hydride reduction (LiAIH, in EtzO or NaBH, in i-PrOH) affords 2,3,4,6,7,8-hexahydro-5H-l-benzopyran-5-ones 5 in 30-60 % isolated yield. Photochemical red