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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77955Erstellt: 24. Oktober 2026

Ammonia → 4-(5-Chloro-furan-2-ylmethyl)-benzylamine

https://huagongshe.com/de/reaction/77955

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktAluminum(III) ChlorideHCID 6451240—
EduktAluminium lithium hydrideHCID 21226445—
Edukt4-((5-Chloro-furan-2-yl)-hydroxy-methyl)-benzonitrileHCID 59255116—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(5-Chloro-furan-2-ylmethyl)-benzylamineHCID 5925539785,6%

Reaktionsschritte

To a mixture of lithium aluminum hydride (3.3 g, 69 mmol) and tetrahydrofuran (100 mL) was added aluminum chloride (13 g, 96 mmol) at 0° C., which was stirred for 1 hour at room temperature. A mixture of 4-((5-chloro-furan-2-yl)-hydroxy-methyl)-benzonitrile (3.2 g) described in Manufacturing Example 62-1-1 and tetrahydrofuran was added dropwise into the reaction mixture, and stirred for 1 hour at room temperature. A 28% aqueous ammonia solution was added dropwise into the reaction mixture at 0° C. to quench the excess reagent. The reaction mixture was allowed to room temperature and filtered through a Celite pad. The solvent was evaporated from the filtrate under a reduced pressure, and the residue was filtered after addition of diethyl ether. The filtrate was concentrated under a reduced pressure to obtain the title compound (2.6 g) as a crude product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841327B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-0bd1bfac91b847a89dc74bd1a789f219
Quellennotizuspto-grants-2014_09