HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937034Generated: October 26, 2026
Phenylacetic Acid → N-hydroxy-2-phenylacetamide
https://huagongshe.com/reaction/1937034
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylacetic Acid | HCID 999 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Product | N-hydroxy-2-phenylacetamide | HCID 220184 | 39% |
Reaction Steps
To a suspension of the 4-(methyl-O-methylhydroxylamine)-2-fluorophenoxymethyl-copoly(styrene-1% divinylbenzene)resin (0.10 g, 0.14 mmol) in dry DMF (2 ml) is added 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.08 g, 0.42 mmol, 3 eq.). To the mixture is then added phenylacetic acid (0.06 g, 0.42 mmol, 3 eq.). The mixture is shaken overnight. The resin is filtered and washed with DMF (×5), THF: H2O (3:1, ×5), THF (×3), MeOH (×3) and DCM (×3). To the resin is added TFA (1 ml) and DCM (1 ml) and the mixture shaken for 1 hour. The mixture is filtered into a tared vial and the resin washed with DCM (×2) and toluene (×2). The combined filtrates are evaporated in vacuo to yield N-hydroxy-phenyl-acetamide (0.0084 g, 39%). LCMS gives 151 [M+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06392010B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-5bf10fc4d4e54836a3efba8ef0e475dd |
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| Source note | uspto-grants-2002_05 |
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