HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77429Erstellt: 23. Oktober 2026
Acetone → 1-(Tert-butoxycarbonyl)-4-[2,6-difluoro-4-(benzyloxycarbonyl)aminophenyl]piperazine
https://huagongshe.com/de/reaction/77429
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | Benzyl chloroformate | HCID 10387 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | tert-Butyl 4-(4-amino-2,6-difluorophenyl)piperazine-1-carboxylate | HCID 45925741 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(Tert-butoxycarbonyl)-4-[2,6-difluoro-4-(benzyloxycarbonyl)aminophenyl]piperazine | HCID 21462617 | 90% |
Reaktionsschritte
To a solution of 4-(4-amino-2,6-difluoro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (Intermediate III) (25 g, 0.08 mol), in 1:1 acetone:water (300 mL) was added sodium bicarbonate (15.1 g, 0.18 mol). The resulting solution was cooled to 0° C. and benzyl chloroformate (40 mL, 0.24 mol, 50% solution in toluene) was added dropwise. The reaction mixture was stirred at r.t. and progress of the reaction was monitored by TLC. On completion, solvent was evaporated under reduced pressure and the residue was dissolved in ethyl acetate (500 mL). The organic layer was washed with water (2×50 mL), brine (100 mL), dried over anhydrous sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (silica gel, 2:3 ethyl acetate:Pet. ether) to provide title compound (32 g, 90%) as off white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841306B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-30f02fab636b452cb88bf9d04bc20bcf |
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| Quellennotiz | uspto-grants-2014_09 |
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