HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031678Generated: October 27, 2026
Water → 3-formyl-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-one
https://huagongshe.com/reaction/1031678
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 2-(2-Hydroxy-4-methylsulfonylamino-5-phenoxybenzoyl)acetaldehyde | HCID 15107923 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-formyl-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-one | HCID 14722439 | 50.4% |
Reaction Steps
25 g of 2-(2-hydroxy-4-methylsulfonylamino-5-phenoxybenzoyl)acetaldehyde was dissolved in 260 ml of benzene and 130 ml of N,N-dimethylformamide. Thereto was added 26 ml of N,N-dimethylformamide dimethylacetal. The mixture was stirred for 8 hours at room temperature. The reaction mixture was introduced into a mixture consisting of 200 ml of ethyl acetate and 200 ml of water. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried with anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The resulting oily matter was purified by a column chromatography (eluant: a 20 : 1 mixture of toluene and ethyl acetate) to obtain 13 g (yield: 50.4%) of 3-formyl-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04954518 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-cf438d8943ad4266a4ec923102e1089f |
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| Source note | uspto-grants-1990_09 |
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