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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant2-(2-Hydroxy-4-methylsulfonylamino-5-phenoxybenzoyl)acetaldehydeHCID 15107923—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
Product3-formyl-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-oneHCID 1472243950.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954518
Source datasetuspto-grants-1990_09
ORD IDord-cf438d8943ad4266a4ec923102e1089f
Source noteuspto-grants-1990_09