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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195923Generated: November 1, 2026

Ethenesulfonyl fluoride → HCID 131717351, compound

https://huagongshe.com/reaction/1195923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthenesulfonyl fluorideHCID 69612—
ReactantEthanone, 1-(2-amino-4,5-dimethoxyphenyl)-HCID 602085—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
ProductHCID 131717351HCID 13171735185%

Reaction Steps

To a mixture of 2-amino-4,5-dimethoxyacetophenone (18 g, 92 mmol) in 125 mL of glacial acetic acid was added in one portion ethenesulfonyl fluoride (11.4 g, 0.1 mol) under nitrogen. After stirring for 1 hour at room temperature the resulting yellow mixture was refluxed for 1 hour. The yellow crystalline solid was diluted with an equal volume of ether, filtered, washed with ether, and air dried. There was obtained the title compound (23.7 g, 85% yield) as a yellow solid, mp 142.5°-146.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112866
Source datasetuspto-grants-1992_05
ORD IDord-26e1bba136e142fd86be912ef49dc591
Source noteuspto-grants-1992_05