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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465507Generated: October 30, 2026

Ethyl Acetate → HCID 14404121, compound

https://huagongshe.com/reaction/465507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 19875046HCID 19875046—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductHCID 14404121HCID 14404121—

Reaction Steps

A solution of [3-(1-hydroxyethyl)phenylsulphonyl]nitromethane (1.10 g, 4.5 mmol) in dichloromethane (10 ml) was added to a vigorously stirred suspension of pyridinium chlorochromate (1.45 g, 6.7 mmol) in dichloromethane (10 ml). The mixture was stirred for 2 hours. Ethyl acetate (100 ml) was added and the solvent was decanted. The black residue was washed twice with ethyl acetate. The extracts and the decanted solution were combined and filtered through magnesium silicate [`Florisil` (trade mark)]. The solvent was evaporated. The residual yellow solid was recrystallised from toluene to give (3-acetylphenylsulphonyl)nitromethane, as a solid, (0.67 g), m.p. 99°-100° C., microanalysis, found: c, 44.7; H, 3.8; N, 5.7%; C9H9NO5S requires: C, 44.4; H, 3.7; N, 5.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153227
Source datasetuspto-grants-1992_10
ORD IDord-9f36e81ae7204468b7f93aa60f817e7c
Source noteuspto-grants-1992_10