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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905131Generated: November 2, 2026

4-Toluenesulfonyl chloride → HCID 19848776, compound

https://huagongshe.com/reaction/1905131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantHCID 131714023HCID 131714023—
SolventDichloromethaneHCID 6344—
ProductHCID 19848776HCID 19848776—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To 20 ml of methylene chloride is added 346 mg (1 mmole) dl-5-hydroxy-3-(2-aminoethyl)-7-(1,1-dimethylheptyl)-2,2-dimethyl-1,2,3,4-tetrahydroquinoline and 0.166 ml (1.2 mmole) triethylamine. The solution is cooled to -20° C. and a solution of ;b 191 mg (1 mmole) p-toluenesulfonyl chloride in 10 ml methylene chloride is added dropwise over ten minutes. The mixture is allowed to warm to 0° C., poured into ice/water and the layers separated. The aqueous layer is extracted with fresh methylene chloride, the combined organic layers washed with water, saturated sodium bicarbonate solution, brine and dried over anhydrous magnesium sulfate. Evaporation of solvent affords the crude product which is purified by chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04841078
Source datasetuspto-grants-1989_06
ORD IDord-13641822dfc14c72ab80cc3d0118b245
Source noteuspto-grants-1989_06