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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080254Generated: October 25, 2026

5-Benzylfuran-2-carbaldehyde → 5-(Phenylmethyl)-2-furanmethanamine

https://huagongshe.com/reaction/2080254

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzylfuran-2-carbaldehydeHCID 12418537—
ReactantAmmonia methanolHCID 21705897—
CatalystNickelHCID 935—
Product5-(Phenylmethyl)-2-furanmethanamineHCID 2313062065.8%

Reaction Steps

7N Ammonia/methanol(40 mL) and Raney nickel(3 g) were added to 5-benzyl-furan-2-carbaldehyde described in Preparation Example 39 (2.5 g, 13 mmol), and the solution was stirred for 22 hours under hydrogen atmosphere at room temperature. After removing the catalyst by filtering through Celite pad, the solvent was evaporated in vacuo and C-(5-benzyl-furan-2-yl)methylamine (1.6 g, 8.6 mmol, 65.8%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-fa9049e0f9524da9bf4ee48ab4ee6885
Source noteuspto-grants-2011_04