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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640238Generated: October 27, 2026

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

https://huagongshe.com/reaction/640238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant4-((5-Chloro-furan-2-yl)-hydroxy-methyl)-benzonitrileHCID 59255116—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Chloro-furan-2-ylmethyl)-benzylamineHCID 5925539785.6%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-bed8027813354262aed02f8278a74050
Source noteuspto-grants-2010_04