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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031667Generated: October 31, 2026

Methanol → HCID 14722453, compound

https://huagongshe.com/reaction/1031667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 10621601HCID 10621601—
CatalystSilver tetrafluoroborateHCID 159722—
ProductHCID 14722453HCID 1472245335%

Reaction Steps

There were mixed 4.12 g of 3-bromo-2,3-dihydro-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-one, 9.37 g of silver tetrafluoroborate and 100 ml of methanol. The mixture was refluxed for 4 hours. The reaction mixture was cooled and filtered to remove the insolubles. The filtrate was subjected to distillation under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluant: a 5 : 1 mixture of toluene and ethyl acetate) to obtain 1.27 g (yield: 35%) of 2,3-dihydro-3-methoxy-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-3236888891234dd3bdc986e52efe8ff2
Source noteuspto-grants-1990_09