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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073754Generated: October 30, 2026

Tetrahydrofuran → HCID 19855948, compound

https://huagongshe.com/reaction/2073754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 3060773HCID 3060773—
Reactant4-[(Methylsulfonyl)amino]benzoyl chlorideHCID 11791119—
SolventAcetonitrileHCID 6342—
ProductHCID 19855948HCID 19855948—

Reaction Steps

To 15 mL of tetrahydrofuran under nitrogen atmosphere add 0.74 g (4.7 mmol) of 4-[(methylsulfonyl)amino]benzoyl chloride then add 0.89 g (0.40 mmol) of N,N-diethyl-N'-(2,6-dimethylphenyl)-1,2-ethanediamine. When the addition is complete allow the reaction to stir at reflux. Monitor the progress of the reaction by thin-layer chromatography (concentrated aqueous ammonium hydroxide: acetonitrile, 1:9). Upon completion of the reaction, cool the mixture to room temperature. Filter the resulting solid and wash the solid with tetrahydrofuran. Recrystallize from acetonitrile to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920116
Source datasetuspto-grants-1990_04
ORD IDord-bd46b3759fbe4614aab8371a7b87183b
Source noteuspto-grants-1990_04