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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444611Generated: October 27, 2026

3-[(Triphenylmethyl)sulfanyl]propanoic acid → 11-(p-Tolyloxy)undecyl 3-(tritylthio)propioate

https://huagongshe.com/reaction/444611

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(Triphenylmethyl)sulfanyl]propanoic acidHCID 262767—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant11-(p-Tolyloxy)undecan-1-olHCID 67541960—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product11-(p-Tolyloxy)undecyl 3-(tritylthio)propioateHCID 67542046—

Reaction Steps

The compound 14 (1.86 g), 0.896 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC), and 0.029 g of 4-dimethylaminopyridine (DMAP) were dissolved in 300 ml of methylene chloride. After the compound 16 (3.04 g) was then added and stirred at room temperature for 24 hours, the reaction solution was moved into a separating funnel, and was washed twice with 100 ml of 10% aqueous potassium hydrogen sulfate solution, twice with 100 ml of aqueous saturated sodium hydrogen carbonate solution, twice with 100 ml of ion-exchange water, and twice with 100 ml of saturated brine. After the methylene chloride phase collected was dehydrated with magnesium sulfate, the desiccant agent was removed by filtration, and the solvent of the filtrate was distilled away under reduced pressure. The reaction mixture was purified by chromatography, and 2.63 g of 11-(p-tolyloxy)undecyl 3-(tritylthio)propioate 17, which was a white solid, was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08475685B2
Source datasetuspto-grants-2013_07
ORD IDord-245c61df200e46fc9b62c262e5ea641a
Source noteuspto-grants-2013_07