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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23958Erstellt: 23. Oktober 2026

1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid → Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/de/reaction/23958

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
EduktBorane;tetrahydrofuranHCID 2723981—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 276408185%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

1-Boc-isonipecotic acid (10.0 g, 214 mmol) was dissolved in THF (400 mL) and cooled to 0° C. A solution of BH3-THF (180 mL, 1 N in THF, 180 mmol) was added slowly. The mixture stirred for 1 h at 0° C. and was allowed to warm to room temperature for 12 h. The mixture was carefully quenched with water and diluted with ethyl acetate. The water layer was extracted with ethyl acetate. The organic layers were combined, washed with brine, dried (Na2SO4), filtered and concentrated to provide l-Boc-piperidine-4-methanol (7.98 g, 85%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855715B1
Quelldatensatzuspto-grants-2005_02
ORD IDord-69907c3ae526490195aad8c034f65fdb
Quellennotizuspto-grants-2005_02