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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221166Generated: October 30, 2026

1-Pyrrolidineethanol → HCID 69209252, compound

https://huagongshe.com/reaction/2221166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PyrrolidineethanolHCID 76288—
ReactantHydroxide, hydrateHCID 445487—
ReactantHCID 69206561HCID 69206561—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 69209252HCID 692092520.3%

Reaction Steps

To a solution of 4-[2-(3-benzofuran-2-yl-4-bromobut-2-enoylamino)ethoxy]benzoic acid methyl ester (300 mg, 0.654 mmol) in dry DMF (4 ml), cessium hydroxide monohydrate (121 mg, 0.72 mmol), tetrabutylammonium iodide (49 mg, 0.13 mmol) and 1-(2-hydroxy-ethyl)pyrrolidine (85 ul, 0.72 mmol) were added. The reaction mixture was stirred overnight at rt and then diluted with EA (20 ml) and washed with water and brine. After drying over sodium sulfate, the solvent was evaporated under vacuum and the crude was purified on preparative TLC, DCM/MeOH (9/1) to give 4-{2-[3-benzofuran-2-yl-4-(2-pyrrolidin-1-yl-ethoxy)but-2-enoylamino]ethoxy}benzoic acid methyl ester (0.94 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368476B2
Source datasetuspto-grants-2008_05
ORD IDord-6257d0facfd54f5a81f3c31c5b18d50b
Source noteuspto-grants-2008_05