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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2168660Erstellt: 26. Oktober 2026

Ammonium Chloride → tert-Butyl 4-hydroxy-3-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2168660

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktSodium borohydrideHCID 4311764—
Edukt1-(1,1-Dimethylethyl) 3-ethyl 4-oxo-1,3-piperidinedicarboxylateHCID 6420876—
LösungsmittelMethanolHCID 887—
Produkttert-Butyl 4-hydroxy-3-(hydroxymethyl)piperidine-1-carboxylateHCID 6671785684,6%

Reaktionsschritte

To a stirred solution of 4-oxo-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (14 g) in MeOH (300 mL) was added NaBH4 (12 g) in 12 lots over 1 h period. After completion of addition, the reaction mixture was stirred for 30 min. Removed solvent under reduced pressure, to the residue was added saturated NH4Cl solution (300 mL) and was extracted with EtOAc (300 mL). The organic layer was dried, filtered and concentrated under reduced pressure. The residue was purified by flash silica gel column chromatography by eluting with ethyl acetate to give 4-hydroxy-3-hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (10.1 g, cis/trans mixture).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09045461B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-601b0b9f551647ccbbf67337d1eab512
Quellennotizuspto-grants-2015_06