Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260266Generated: November 1, 2026

Triethylamine → HCID 53628723, compound

https://huagongshe.com/reaction/1260266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Propan-2-yl)benzene-1-sulfonyl chlorideHCID 2734882—
ReactantHCID 57494449HCID 57494449—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53628723HCID 53628723129.7%

Reaction Steps

4-(1-Benzyl-pyrrolidin-3-yl)-2-methoxy-phenylamine (220 mg, 0.78 mmol) and 4-isopropylphenylsulfonyl chloride (170 mg, 0.78 mmol) were dissolved in tetrahydrofuran (20 ml). Triethylamine (0.32 ml, 2.34 mmol) was added and the reaction mixture stirred over night at room temperature (10% conversion) and subsequently refluxed for 4 h (70% conversion). One small portion of 4-isopropylphenylsulfonyl chloride and triethylamine were added and the reaction mixture was stirred 15 min at 150° C. in the microwave (CEM). The solvent was evaporated under reduced pressure, the residue treated with ethyl acetate (50 ml) and extracted twice with slightly acidic water. The organic layer was dried over magnesium sulfate, filtered, and the solvent evaporated under reduced pressure to give an oil (470 mg). The crude product was purified via silica gel chromatography with cyclohexane/ethyl acetate (gradient 0-100%). Fractions containing the product were combined, the solvent evaporated to yield an oil (143 mg, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470810B2
Source datasetuspto-grants-2013_06
ORD IDord-6dccb04164fc493592477dcf8294c375
Source noteuspto-grants-2013_06