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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1046299Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1046299

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
PatentnummerUS08569303B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-a4af34579fff4ba78e1753f5c4d0274e
Quellennotizuspto-grants-2013_10