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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Edukttert-butyl N-[(2-aminophenyl)methyl]carbamateHCID 4409487—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelChloroformHCID 6212—
ProduktTert-butyl (2-(tert-butoxycarbonylaminomethyl)anilino)piperidine carboxylateHCID 54015391106,4%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05691323
Quelldatensatzuspto-grants-1997_11
ORD IDord-4aad9fe7b0b14412bd4f2c4209e19d89
Quellennotizuspto-grants-1997_11