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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60250Erstellt: 24. Oktober 2026

Formaldehyde → (R)-tert-butyl 3-(hydroxymethyl)-4-methylpiperazine-1-carboxylate

https://huagongshe.com/de/reaction/60250

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktSodium CarbonateHCID 10340—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukttert-Butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820286—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-tert-butyl 3-(hydroxymethyl)-4-methylpiperazine-1-carboxylateHCID 58365052—

Reaktionsschritte

To a solution of (R)-tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (115 mg, 0.53 mmol) in acetonitrile (1.4 mL) and water (0.3 mL) was added Formalin (0.11 mL, 1.6 mmol) followed by sodium triacetoxyborohydride (225 mg, 1.1 mmol). The reaction mixture was stirred for 20 minutes at ambient temperature. The reaction mixture was then basified via the addition of saturated aqueous sodium carbonate solution (1 mL), diluted with methylene chloride (50 mL) and methanol (5 mL), and washed with saturated aqueous sodium bicarbonate solution (2×15 mL). The organic layer was separated, dried over sodium sulfate, and concentrated in vacuo to afford a white crystalline solid, which was used in the next step without any further purification (120 mg, 98%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440976B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-209d4574534a4c8dbaebce40c777f396
Quellennotizuspto-grants-2016_09