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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTrifluoroacetamideHCID 67717—
ReactantMagnesium monoxideHCID 6850729—
ReactantIodo benzene diacetateHCID 12217721—
ReactantMethyl 3-(methylsulfinyl)benzoateHCID 57657958—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-[imino(methyl)oxo-lambda6-sulfanyl]benzoateHCID 5765795774.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383825B2
Source datasetuspto-grants-2013_02
ORD IDord-12236423dfad4ef6b6ec8cd9be922a80
Source noteuspto-grants-2013_02