HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391597Generated: October 29, 2026
Potassium Carbonate → Methyl 3-[imino(methyl)oxo-lambda6-sulfanyl]benzoate
https://huagongshe.com/reaction/391597
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trifluoroacetamide | HCID 67717 | — |
| Reactant | Magnesium monoxide | HCID 6850729 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | Methyl 3-(methylsulfinyl)benzoate | HCID 57657958 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-[imino(methyl)oxo-lambda6-sulfanyl]benzoate | HCID 57657957 | 74.2% |
Reaction Steps
A solution of methyl 3-(methylsulfinyl)benzoate (3.23 g, 16.3 mmol), 2,2,2-trifluoroacetamide (3.69 g, 32.6 mmol), magnesium oxide (1.97 g, 48.9 mmol), rhodium(II)acetate dimer (0.18 g, 0.408 mmol), and iodobenzene diacetate (7.88 g, 24.5 mmol) in 150 ml dichloromethane was stirred at room temperature. After 16 hours, the mixture was filtered past filter agent (Celite), rinsed with chloroform, and rotary evaporated. The sample was dissolved in EtOAc, washed with brine/dilute HCl, brine, dried with anhydrous Na2SO4 and rotary evaporated. The yellow-orange oil was dissolved in 60 ml MeOH, K2CO3 (6.76 g, 48.9 mmol) added, and the mixture stirred at room temperature for 12 minutes. The MeOH filtrate was decanted from the solids, which were then rinsed with MeOH and EtOAc. The pH of the combined organic filtrates were adjusted to pH 2 using 4% HCl, then the aqueous layer diluted by adding H2O. The aqueous layer was washed with 30% EtOAc in hexane, then the pH adjusted to pH 9 with saturated Na2CO3. The aqueous layer was extracted with CHCl3, the combined CHCl3 layers washed with brine, dried with anhydrous Na2SO4 and rotary evaporated to give the title compound as a light tan solid (2.58 g, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383825B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-12236423dfad4ef6b6ec8cd9be922a80 |
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| Source note | uspto-grants-2013_02 |
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