Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 4-Ethyl-2-(4-nitrophenyl)morpholine | HCID 57416112 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 4-(4-Ethylmorpholin-2-yl)aniline | HCID 57416068 | — |
Reaction Steps
Combined 4-Ethyl-2-(4-nitro-phenyl)-morpholine (3.00 g, 0.0127 mol) with Methanol (300 mL, 6 mol) and add Ammonium formate (5.6 g, 0.089 mol) then 10% Pd/C, 50% wet (0.88 g, 0.00041 mol). Stir under N2 overnight. Filtered through Celite and concentrated. Partitioned between aq. Na2CO3 and EtOAc, the organics were dried (MgSO4), filtered. To give 4-(4-Ethyl-morpholin-2-yl)-phenylamine as yellowish oil which solidified upon standing (2.45 grams). 1H-NMR (CDCl3) δ 7.17 (d, J=8.4 Hz, 2H), 6.68-6.65 (m, 2H), 4.47 (dd, J=10.4, 2.3 Hz, 1H), 4.05-4.01 (m, 1H), 3.90-3.84 (m, 1H), 3.84 (dt, J=11.6, 2.4 Hz, 1H), 3.66 (broad s, 2H), 2.94-2.90 (m, 1H), 2.84-2.81 (m, 1H), 2.46 (q, J=7.2, 2H), 2.2 (dt, J=8.1, 11.5 Hz, 1H), 2.05 (t, J=11.0 Hz, 1H), 1.12 (t, J=7.2 Hz, 1H); LC/MS (ESI+): 207 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08471005B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-bc65dc5f6a1d4d10b6e91cfd96c5ba5f |
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| Source note | uspto-grants-2013_06 |
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