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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 471048Erstellt: 25. Oktober 2026

Ethyl bromodifluoroacetate → tert-Butyl 4-((2-bromo-2,2-difluoroacetamido)methyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/471048

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromodifluoroacetateHCID 69585—
Edukttert-Butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylateHCID 23396319—
LösungsmittelDimethylformamideHCID 6228—
Produkttert-Butyl 4-((2-bromo-2,2-difluoroacetamido)methyl)-4-hydroxypiperidine-1-carboxylateHCID 57988980—

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A solution of tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate (1.702 g) in DMF (20 mL) at 20° C. was treated with ethyl 2-bromo-2,2-difluoroacetate (1.5 g) and the mixture stirred for 90 minutes at 20° C. under nitrogen. The mixture was partitioned between ethyl acetate and brine, the organic layer was washed twice with brine, dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure to afford the subtitled compound. Yield 2.5 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629271B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-435b4c8bbeae44fe81601b8d05ad124c
Quellennotizuspto-grants-2014_01