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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 630323Erstellt: 26. Oktober 2026

Acetic Acid → 1,1-Dimethylethyl 2-((4-(methoxycarbonyl)phenylmethylamino)methyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/630323

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktMethyl 4-FormylbenzoateHCID 15294—
Edukttert-Butyl 2-(aminomethyl)piperidine-1-carboxylateHCID 2756482—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelWaterHCID 962—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt1,1-Dimethylethyl 2-((4-(methoxycarbonyl)phenylmethylamino)methyl)-1-piperidinecarboxylateHCID 6848915796,6%

Reaktionsschritte

A solution of 1-Boc-2-aminomethylpiperidine (429 mg, 2 mmol) and methyl 4-formylbenzoate (329 mg, 2 mmol) in dichloroethane (10 mL) was stirred as acetic acid (180 mg, 3 mmol) and sodium triacetoxyborohydride (487 mg, 2.3 mmol) were added sequentially. The reaction was stirred at ambient temperature for 17 hours. The reaction was poured into water and extracted with methylene chloride (2×). The organic phase was dried over sodium sulfate, filtered, and concentrated. Purification on silica gel using a gradient of ethyl acetate in hexane gave 0.7 g of 1,1-dimethylethyl 2-((4-(methoxycarbonyl)phenylmethylamino)methyl)-1-piperidinecarboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09315509B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-5fbca0966e384267abbd1bb71d88c92e
Quellennotizuspto-grants-2016_04