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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476791Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 3090868, compound

https://huagongshe.com/reaction/476791

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantN'-(2-aminoethyl)-N'-benzylethane-1,2-diamineHCID 10081318—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 3090868HCID 309086879.3%

Reaction Steps

To a solution of 141.2 g (0.741 mol) of p-toluenesulfonyl chloride in 250 ml of dichloromethane with 110 ml (0.8 mol) of triethylamine was added dropwise 68.0 g (0.352 mol) of 4-benzyl-1,4,7-triazaheptane in 75 ml of dichloromethane. After 2 hours, the solution was washed three times with water at pH 9, and the organic phase was dried with sodium sulfate and filtered. Evaporation gave an oil which was dissolved in about 450 ml of ethyl acetate. The solution was diluted with 200 ml of ether and left to stand at room temperature for 24 hours. The mixture was further diluted with about 50 ml of ether and refrigerated for another day. The product crystallized in massive prisms which were collected by filtration and dried under vacuum at 40° C. for 6 hours, yielding in the first crop 140 g (0.279 mol) of a colorless solid; melting point 87°-91° C. Mass spectrum (CI): m/e 502 (M+H) and 500 (M-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885363
Source datasetuspto-grants-1989_12
ORD IDord-7d48a75f9aeb4e839e477e1efcc667a0
Source noteuspto-grants-1989_12