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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615674Generated: October 30, 2026

1,2,3,4-Tetrahydro-6-nitronaphthalene → 5,6,7,8-Tetrahydro-2-naphthylamine

https://huagongshe.com/reaction/1615674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-Tetrahydro-6-nitronaphthaleneHCID 88018—
Reactant1,2,3,4-Tetrahydro-5-nitronaphthaleneHCID 93130—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5,6,7,8-Tetrahydro-2-naphthylamineHCID 7519340%

Reaction Steps

To a solution of 6-nitro-1,2,3,4-tetrahydronaphthalene and 5-nitro-1,2,3,4-tetrahydronaphthalene (5.5 g, 31.1 mmol) in MeOH (50 mL) was added 10% palladium on carbon (3.18 g, 3.0 mmol) under nitrogen, then replaced with hydrogen atmosphere (2 L). The resulting mixture was stirred at room temperature for 16 h, and filtered through Celite. The filtrate was concentrated, and the residue was purified by silica gel column (PE/EtOAc v/v 10:1) to give 5,6,7,8-tetrahydronaphthalen-2-amine as a white solid (2 g, 40% yield). ESI MS: m/z 148 [M+H]+. 1H NMR (400 MHz, CDCl3): δ 6.88 (d, J=8.0 Hz, 1H), 6.49 (dd, J=2.0 Hz, J=8.0 Hz, 1H), 6.44 (d, J=2.0 Hz, 1H), 3.49 (s, 2H), 2.69-2.67 (m, 4H), 1.78-1.75 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765760B2
Source datasetuspto-grants-2014_07
ORD IDord-bb20b5932f8648d2b156cc61b9972817
Source noteuspto-grants-2014_07