HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424418Generated: October 30, 2026
Methanol → N-(4-((2S)-morpholin-2-yl)phenyl)acetamide
https://huagongshe.com/reaction/424418
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | N-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)acetamide | HCID 66594393 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4-((2S)-morpholin-2-yl)phenyl)acetamide | HCID 66594379 | 131.2% |
Reaction Steps
To a solution of N-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)acetamide (6.47 g, 20 mmol) and ammonium formate (6.3 g, 100 mmol) in mixture of tetrahydrofuran (136 ml), methanol (270 ml) and water (70 ml) was added 10% palladium on carbon (wet, 270 mg) and the solution was stirred at 95° C. for 3 hours. After filtration, the solvent was removed in vacuo and the residue was partitioned between water and dichloromethane. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give N-(4-((2S)-morpholin-2-yl)phenyl)acetamide (5.78 g, quant.) as an yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106045B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-6b3c2f1e2e894992935e88bf27aeb62a |
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| Source note | uspto-grants-2012_01 |
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