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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987773Generated: October 30, 2026

4-Toluenesulfonyl chloride → 1-(3-(1-Pyrrolidinyl)propyl)-3-ethylcarbodiimide

https://huagongshe.com/reaction/987773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantN-ethyl-N'-3-(1-pyrrolidinyl)propylureaHCID 15871432—
SolventDichloromethaneHCID 6344—
Product1-(3-(1-Pyrrolidinyl)propyl)-3-ethylcarbodiimideHCID 1013023267%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 31.0 g (0.156 mol) N-ethyl-N′-3-(1-pyrrolidinyl)propylurea in 500 mL dichloromethane was added 62.6 g (0.62 mol) triethylamine and the solution was cooled to 0° C. To this solution were then added 59.17 g (0.31 mol) 4-toluenesulfonyl chloride in 400 mL dichloromethane dropwise at such a rate as to maintain the reaction at 0-5° C. After the addition was complete, the reaction mixture was warmed to room temperature and then heated to reflux for 4 hours. After cooling to room temperature, the reaction mixture was washed with saturated aqueous potassium carbonate (3×150 mL). The aqueous phases were combined and extracted with dichloromethane. All organic phases were combined and concentrated under reduced pressure. The resultant orange slurry was suspended in 250 mL diethyl ether and the solution decanted off from the solid. The slurry/decantation process was repeated 3 more times. The ether solutions were combined and concentrated under reduced pressure to give 18.9 g (67%) of the desired product as a crude orange oil. A portion of the oil was distilled under vacuum to give a colorless oil distilling at 78-82° C. (0.4 mm Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06632811B2
Source datasetuspto-grants-2003_10
ORD IDord-c29d096237be442f8a69d4497c18508f
Source noteuspto-grants-2003_10