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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307406Generated: November 1, 2026

1,4-Benzodioxan-6-yl methyl ketone → 1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethanamine

https://huagongshe.com/reaction/2307406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Benzodioxan-6-yl methyl ketoneHCID 76143—
ReactantAmmonium hydroxide methanolHCID 21894508—
CatalystNickelHCID 935—
SolventHydrochloric AcidHCID 313—
Product1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethanamineHCID 314611166%

Reaction Steps

A mixture of 1-(2,3-dihydro-1,4-benzodioxin-6-yl)acetaldehyde, oxime, (Preparation 5, 10.74 g, 0.0556 mole), and Raney nickel (1 mL) in ammonium hydroxide/methanol (20 mL/200 mL) was hydrogenated (H2, 50 psi) for 48 hours. The reaction mixture was filtered through Celite and the resultant filtrate was concentrated in vacuo. The residual oil obtained was diluted with HCl (1N). The aqueous layer was washed with EtOAc (1×250 mL). The aqueous layer was then made basic with NaOH (1N), and extracted with EtOAc (3×200 mL). The combined organic layers were dried over anhydrous magnesium sulfate, filtered and the resultant filtrate was concentrated in vacuo to provide the title product (7.1 g, 66%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831080B2
Source datasetuspto-grants-2004_12
ORD IDord-d967f24a6a3a4a9fa0204c971aadbe38
Source noteuspto-grants-2004_12