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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1486695Erstellt: 25. Oktober 2026

m-Nitroacetophenone → HCID 131736797, Verbindung

https://huagongshe.com/reaction/1486695

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-NitroacetophenoneHCID 8494—
EduktSodium borohydrideHCID 4311764—
Eduktn-Cyclohexylpiperidine-4-carboxamideHCID 12410238—
LösungsmittelMethanolHCID 887—
ProduktHCID 131736797HCID 13173679715%

Reaktionsschritte

Piperidine-4-carboxylic acid cyclohexylamide (1.5 g 7.132 mmol) and 3-nitroacetophenone (1.77 g, 10.7 mmol) are dissolved in MeOH (40 mL). Tetraisopropyl-orthotitanate (3.167 mL, 10.7 mmol) is added and the mixture is stirred at RT for 18 h. NaBH4 (539.6 mg, 14.3 mmol) is added carefully. The mixture is evaporated under reduced pressure. DCM (25 mL) and water (25 mL) are added, following by 1 M NaOH solution (50 mL). The organic phase is separated and the aqueous phase is extracted with DCM (25 mL). The combined organic phases are dried over MgSO4, filtered and concentrated. The crude residue is purified by flash chromatography on silica gel using a gradient of heptane/EtOAc 4:1 to EtOAc 100%. After concentration of the product-containing fractions, the title compound (0.375 g, 15%) is obtained as a colorless solid LC-MS A: tR=0.64 min; [M+H]+=360.26.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09428456B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-40ff7817415c40428cd748c90186e540
Quellennotizuspto-grants-2016_08