## Abstract Tetraarylcyclopentadienones 2a–c react with (__E__)‐3,4,5,6,7‐penta‐__O__‐acetyl‐1,2‐dideoxy‐1‐__C__‐nitro‐D‐__galacto__‐ (1a) and ‐D‐__manno__‐hept‐1‐enitol (1b) to give 1‐__C__‐(2,3,4,5‐tetraarylphenyl)‐D‐__galacto__‐ (3a–c) and ‐D‐__manno__‐penta‐__O__‐acetylpentitol (3d‐f), respecti
Synthesis of 3 or 5[14C] 4-butyl-1, 2-diphenyl-3, 5-pyrazolidinedione (phenylbutazone)
✍ Scribed by S. Stavchansky; H. B. Kostenbauder
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- French
- Weight
- 136 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The condensation of 1 or 3 [^14^C] n‐butylmalonate diethyl ester (III) with hydrazobenzene (IV) yields up to 90 per cent of 3 or 5 [^14^C] 4‐butyl‐1, 2‐diphenyl‐3, 5‐pyrazolidinedione, if n‐butyl alcohol is used as a solvent and the corresponding sodium alcoholate as a condensing agent (1, 2).
One or three [^14^C] n ‐ butylmalonate diethyl ester can be synthesized by condensation of n‐bromobutane (II) and 1 [^14^C] ethyl malonate (I) in the presence of sodium ethoxide (3).
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