HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2294927Erstellt: 25. Oktober 2026
Sodium Carbonate → Tert-butyl (2-(tert-butoxycarbonylaminomethyl)anilino)piperidine carboxylate
https://huagongshe.com/reaction/2294927
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Edukt | tert-butyl N-[(2-aminophenyl)methyl]carbamate | HCID 4409487 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | Tert-butyl (2-(tert-butoxycarbonylaminomethyl)anilino)piperidine carboxylate | HCID 54015391 | 106,4% |
Reaktionsschritte
A mixture of 15.5 g of 2-(tert-butoxycarbonylaminomethyl)aniline, 15 g of N-t-butyloxycarbonyl-4-piperidone, 250 mL of 1,2-dichloroethane, 4.2 mL of glacial acetic acid and 25 g of sodium triacetoxyborohydride was stirred at room temperature for 48 h. The reaction mixture was poured into 500 mL chloroform and 500 mL saturated aqueous Na2CO3 and the layers separated. The aqueous layer was extracted with 2×250 mL of chloroform and the combined organic layers dried over MgSO4 and concentrated under reduced pressure. Drying overnight under vacuum gave 30.1 g of tert-butyl (2-(tert-butoxycarbonylaminomethyl)anilino)piperidine carboxylate as a solid: 1H NMR (400 MHz, CDCl3) 7.19 (t, 1H), 7.0 (d, 1H), 6.6 (dd, 2H), 4.94 (br s, 1H), 4.75 (br s, 1H), 4.23 (br m, 2H), 4.0 (br m, 2H), 3.45 (br m, 1H), 3.0 (br m, 2H), 2.0 (br m, 2H), 1.82 (br m, 1H), 1.46 (s, 9H), 1.44 (s, 9H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05691323 |
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| Quelldatensatz | uspto-grants-1997_11 |
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| ORD ID | ord-4aad9fe7b0b14412bd4f2c4209e19d89 |
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| Quellennotiz | uspto-grants-1997_11 |
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