Technology Process of 4-bromo-2-nitro-6-tetrahydrofuran-2-yl-aniline
There total 6 articles about 4-bromo-2-nitro-6-tetrahydrofuran-2-yl-aniline which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
sodium hydroxide;
In
1,4-dioxane; water;
for 48h;
Reflux;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: potassium carbonate / palladium diacetate; (R)-1-[(S)-2-(diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine ethanol adduct / 1,4-dioxane / 105 °C / Inert atmosphere; Sealed tube
1.2: 20 °C / 1551.49 Torr
2.1: N-Bromosuccinimide / acetonitrile; tert-butyl methyl ether / 0.5 h / 2 - 8 °C
3.1: ammonium nitrate / 2-methyltetrahydrofuran / 1.42 h / 2 - 40 °C
4.1: sodium hydroxide; water / 1,4-dioxane / 48 h / Reflux
With
N-Bromosuccinimide; ammonium nitrate; water; potassium carbonate; sodium hydroxide;
(R)-1-[(S)-2-(diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine ethanol adduct; palladium diacetate;
In
2-methyltetrahydrofuran; 1,4-dioxane; tert-butyl methyl ether; acetonitrile;
1.1: Heck coupling;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: N-Bromosuccinimide; sodium thiosulfate / tert-butyl methyl ether
2: trifluoroacetic anhydride; ammonium nitrate
3: NaOH / 1,4-dioxane
With
N-Bromosuccinimide; NaOH; ammonium nitrate; sodium thiosulfate; trifluoroacetic anhydride;
In
1,4-dioxane; tert-butyl methyl ether;