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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852537Generated: October 30, 2026

Water → HCID 69357176, compound

https://huagongshe.com/reaction/852537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-EthylbenzylamineHCID 84352—
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 69358761HCID 69358761—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 69357176HCID 6935717660%

Reaction Conditions

Temperature90 °C

Reaction Steps

A flask was charged under nitrogen with 3-bromo-5-(2-oxo-pyrrolidin-1-yl)-benzoic acid tert-butyl ester (D9b) (4.6 g, 13 mmol, 1 equiv), sodium tert-butoxide (1.9 g, 19.5 mmol, 1.5 equiv), tris(dibenzylideneacetone)dipalladium(0) (395 mg, 0.65 mmol, 0.05 equiv), 2-(dicyclohexylphosphino)biphenyl (341 mg, 0.97 mmol, 0.075 equiv) and toluene (100 ml). N-Ethylbenzylamine (2.9 ml, 19.5 mmol, 1.5 equiv) was then added via syringe and the resulting mixture was stirred at 90° C. for 2 h then cooled to room temperature, diluted with H2O and AcOEt. The layers were separated, the aqueous phase diluted with saturated aqueous NaHCO3 solution and extracted with AcOEt. The combined organic phases were dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (iso-hexane/AcOEt: 1/2) gave (benzyl-ethyl-amino)-(2-oxo-pyrrolidin-1-yl)-benzoic acid tert-butyl ester (D30) (3 g, 60%) as a white solid. [M+H]+=395.0, RT=3.70 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-fee28d37134c45488134fcb826761c2e
Source noteuspto-grants-2007_08