HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750986Generated: October 26, 2026
1-Cyclopentyloxy-2-methoxy-5-nitrobenzene → 3-(Cyclopentyloxy)-4-methoxyaniline
https://huagongshe.com/reaction/750986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Cyclopentyloxy-2-methoxy-5-nitrobenzene | HCID 11390741 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Cyclopentyloxy)-4-methoxyaniline | HCID 2779334 | 95.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405230B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-2e0927ad6b334182a69b62c7395b9e43 |
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| Source note | uspto-grants-2008_07 |
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