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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1984966Erstellt: 27. Oktober 2026

Nitrogen → (S)-Tetrahydrofuran-3-yl (3-aminobenzyl)carbamate

https://huagongshe.com/reaction/1984966

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
Edukt(S)-Tetrahydrofuran-3-yl (3-nitrobenzyl)carbamateHCID 57718888—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(S)-Tetrahydrofuran-3-yl (3-aminobenzyl)carbamateHCID 59901461—

Reaktionsschritte

Charged 15 g of (S)-tetrahydrofuran-3-yl 3-nitrobenzylcarbamate 2c in 120 ml EtOAc to a 1 L Parr bomb at room temperature under a blanket of N2. The agitator was started and the vessel pressurized with N2 to 0.75 bar, then the pressure was released. This procedure was repeated 3 times, then the agitator was stopped before adding 0.225 g of 5% Pd/C. The agitator was started, the vessel pressurized with N2 to 0.75 bar, then the pressure was released. This procedure was repeated 3 times, then the agitator was stopped. The vessel was pressurized with H2 to 2 bar, then the pressure was released. This procedure was repeated 3 times, then the vessel was pressurized with H2 to 6.75 bar. The agitator was started and the suspension stirred until complete conversion was evident by HPLC. The H2 pressure was released, the vessel re-pressurized with N2 to 0.75 bar, then the pressure was released. This procedure was repeated 3 times then the agitator was stopped, the reaction mixture filtered through celite and the filter cake rinsed with 30 ml EtOAc to give crude (S)-tetrahydrofuran-3-yl 3-aminobenzylcarbamate 2d as a solution in EtOAc that was used as is immediately in the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07544810B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-2ef9ba87b3bc4365be7da63e971b94af
Quellennotizuspto-grants-2009_06