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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835872Generated: October 31, 2026

4-Toluenesulfonyl chloride → HCID 87983453, compound

https://huagongshe.com/reaction/1835872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantHCID 23500254HCID 23500254—
SolventDichloromethaneHCID 6344—
ProductHCID 87983453HCID 87983453—

Reaction Steps

A 6.1 g amount of 7,10,13-tri (t-butoxycarbonyl)-7,10,13-triazapentadecanol, 100 mg of dimethylaminopyridine, and 4 ml of triethylamine in 100 ml of CH2Cl2 was stirred at 0° C. Dropwise, 2.64 of tosyl chloride in 20 ml of CH2Cl2 was added at 0° to 5° C. The reaction was then stirred overnight at room temperature and then 100 ml of CH2Cl2 was added. The reaction mixture was washed with 30 ml of 2N HCl, 30 ml of water and 30 ml of brine. The organic layer was dried over MgSO4 and was filtered. The solvent was evaporated and the residue from the filtrate was purified using a silica gel column and eluted with ethyl acetate/hexane (1:2 v/v). About 7.8 g of 7,10,13-tri(t-butoxycarbonyl)-7,10,13-triazapentadecanol tosylate was collected. The reaction is shown below:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06774082B2
Source datasetuspto-grants-2004_08
ORD IDord-ebde50ef3c824edd91bac94568f4a644
Source noteuspto-grants-2004_08