Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 67172733 | HCID 67172733 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67172008 | HCID 67172008 | 87% |
Reaction Steps
To a solution of N-(3-(ethylthiomethyl)phenyl)acetamide (1 g, 5 mmol) in DCM (10 mL) was added mCPBA (2.4 g, 14 mol). The reaction mixture was stirred at 40° C. overnight. Then water was added, the organic layer was separated and washed with an aqueous of NaHCO3, dried over Na2SO4, concentrated and purified by silica gel chromatography (petroleum ether:EtOAc=1:0 to 5:1) to give N-(3-(ethylsulfonylmethyl)phenyl)acetamide (1 g, 87% yield) as a white solid. 1H NMR: (400 MHz, CDCl3) δ 7.84 (s, 1H), 7.61 (s, 1H), 7.41 (d, 1H), 7.24 (t, 1H), 7.14 (d, 1H), 4.14 (s, 2H), 2.90-2.85 (m, 2H), 2.12 (s, 3H), 1.34 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461134B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-7fc3d25744d0461880f60bcf4a4cdf2e |
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| Source note | uspto-grants-2013_06 |
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