Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dinitrophenol | HCID 1493 | — |
| Reactant | HCID 10593784 | HCID 10593784 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10825027 | HCID 10825027 | 79% |
Reaction Steps
A sample of 2-(methanesulfonylamino)-5-(methoxycarbonyl)benzaldehyde trimethylene mercaptal (7.66 g, 0.022 mol) dissolved in N,N-dimethylformamide (4.35 mL) and acetone (39.13 mL) was added over a 5-min period through a dropping funnel to a solution of copper (II) oxide (2.09 g, 0.026 mol), copper (II) chloride (7.0 g, 0.055 mol) in acetone (174.0 mL) and heated at reflux. After 2 h at reflux, thin-layer chromatography analysis (SiO2, EtOAc:hexane 1:1) showed disappearance of the starting material and the appearance of a new slightly higher Rf spot which gave a positive result when sprayed with 2,4-DNP. Upon cooling, the reaction was filtered through Celite and the cake was washed with 10% ethanol in dichloromethane. Water (125 mL) and dichloromethane (150 mL) were added to the filtrate. The layers were partitioned and the water layer extracted 2×100 mL dichloromethane. The combined organic layers were washed twice with water (100 mL), dried (Na2SO4), and filtered. Concentration of the filtrate gave a beige solid which was dried in vacuo to give 4.48 g (79%) of 2-(methanesulfonylamino)-5-(methoxycarbonyl)benzaldehyde, mp 161°-163° C. (ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05602277 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-0953a01196a24ed9b92f0994ce3a095e |
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| Source note | uspto-grants-1997_02 |
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