Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 21997644 | HCID 21997644 | — |
| Product | HCID 21997642 | HCID 21997642 | — |
Reaction Steps
N-(2-Cyanomethylsulfanyl-4-fluoro-phenyl)acetamide (0.43 g) was suspended in glacial acetic acid (2 ml). Hydrogen peroxide (35%, 1 ml) was added and the mixture was stirred at 100° C. for 1 h. Then the mixture was cooled to 0° C. and water (15 ml) was added. After stirring for 10 min a white precipitate was isolated by filtration, washed with water and dried. Recrystallization from 96% ethanol afforded the title compound as white needles, mp 154-157° C.; yield 0.28 g (58%); 1H-NMR (DMSO-d6), δ (ppm): 9.64 (s, 1H, NH), 7.99-7.64 (m, 3H, Ar—H), 5.30 (s, 2H, CH2), 2.08 (s, 3H, CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06232310B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-b25361d00ce14d448e088d3537b8928f |
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| Source note | uspto-grants-2001_05 |
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