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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271375Generated: November 2, 2026

1-Cyclopentyloxy-2-methoxy-5-nitrobenzene → 3-(Cyclopentyloxy)-4-methoxyaniline

https://huagongshe.com/reaction/1271375

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Cyclopentyloxy-2-methoxy-5-nitrobenzeneHCID 11390741—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(Cyclopentyloxy)-4-methoxyanilineHCID 277933495.4%

Reaction Steps

To a suspension of 10% Pd on activated carbon (25 g) in ethanol (4 L), under N2 protection, was added 1-cyclopentyloxy-2-methoxy-5-nitrobenzene (250 g, 1.054 mol). The reaction mixture was degassed under vacuum three times. The reaction mixture was stirred vigorously while hydrogen gas was allowed to flow over the reaction mixture. After 4 h the reaction was complete by TLC (5:1 hex:EA). The reaction mixture was filtered through a pad of celite and the celite was rinsed with additional ethanol. The solvent was removed in-vacuo to obtain 208.38 g (95% yield) of 3-cyclopentyloxy-4-methoxyaniline as a red liquid. 1H NMR (CDCl3) δ 6.85 (d. J=8.4 Hz, 1H), 6.29 (s, 1H), 6.19 (dd, J=2.8, 8.4, 1H), 4.69 (p, J=4.4 Hz, 1H), 3.75 (s, 3H), 3.44 (bs, 2H), 1.90–1.81 (m, 6H), 1.61–1.55 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205320B2
Source datasetuspto-grants-2007_04
ORD IDord-4414c2d090844a91856e7af0e8cd1efc
Source noteuspto-grants-2007_04