HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835872Generated: October 31, 2026
4-Toluenesulfonyl chloride → HCID 87983453, compound
https://huagongshe.com/reaction/1835872
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | HCID 23500254 | HCID 23500254 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87983453 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06774082B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-ebde50ef3c824edd91bac94568f4a644 |
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| Source note | uspto-grants-2004_08 |
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