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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352176Generated: October 31, 2026

Trimethylamine → HCID 21099927, compound

https://huagongshe.com/reaction/1352176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 21099926HCID 21099926—
SolventDichloromethaneHCID 6344—
ProductHCID 21099927HCID 2109992795.9%

Reaction Steps

A 1.2 g of 8-(4′-isopropylanilino)-1,5-dihydroxy-4-nitroanthraquinone and a 1.4 g of tosyl chloride were dissolved in 20 ml of dichloromethane, and a 1.0 ml of trimethylamine was added to the solution and allowed to react for 12 hours at room temperature under stirring. The reaction solution was extracted with adequate amounts of ethyl acetate and 1N-hydrochloric acid to separate into two layers. The extracted organic layer was dried with magnesium sulfate and concentrated. The obtained product was purified by silica gel chromatography to give a 2.0 g of 8-(4′-isopropylanilino)-4-nitro-1,5-bis(p-toluenesulfonyloxy)anthraquinone in a 94% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220465B2
Source datasetuspto-grants-2007_05
ORD IDord-4a9cafc164254acea8606180d11c208d
Source noteuspto-grants-2007_05