HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639642Generated: November 2, 2026
4-(3,4-Dinitrobenzyl)morpholine → 4-Morpholin-4-yl methyl-benzene-1,2-diamine
https://huagongshe.com/reaction/1639642
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(3,4-Dinitrobenzyl)morpholine | HCID 25193310 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Morpholin-4-yl methyl-benzene-1,2-diamine | HCID 66721753 | 98.6% |
Reaction Steps
4-(3,4-Dinitro-benzyl)-morpholine (0.800 Kg, 2.99 mol, 1.0 wt), and ethanol (11.20 L, 14.0 vol) were charged to a suitable flask and stirred at 15 to 25° C. and a vacuum/nitrogen purge cycle was performed three times. 10% Palladium on carbon (10% Pd/C, 50% wet paste, 0.040 Kg, 0.05 wt wet weight) was slurried in ethanol (0.80 L, 1.0 vol) and added to the reaction. The mixture was cooled to 10 to 20° C. and a vacuum/nitrogen purge cycle was performed three times. A vacuum/hydrogen purge cycle was performed three times and the reaction was stirred under a hydrogen atmosphere at 10 to 20° C. Reaction completion was determined by 1H NMR analysis (d6-DMSO), typically 14 to 20 hours. A vacuum/nitrogen purge cycle was performed three times and the reaction mixture was filtered through glass microfibre paper under nitrogen. The filter-cake was washed with ethanol (3×0.80 L, 3×1.0 vol) and the combined filtrate and washes were concentrated to dryness under vacuum at 35 to 45° C. to give 4-morpholin-4-yl-methyl-benzene-1,2-diamine (0.611 Kg 98.6%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110573B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-b3d82893748e48b49013d889a238f3e9 |
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| Source note | uspto-grants-2012_02 |
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