Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727575Generated: November 1, 2026

Diisopropylethylamine → HCID 19705462, compound

https://huagongshe.com/reaction/727575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3,4-Difluorobenzoyl chlorideHCID 2724519—
ReactantHCID 19705530HCID 19705530—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 19705462HCID 19705462137%

Reaction Steps

A cold (0° C.) solution of tert-butyl α-(2-aminoethyl)-2-oxo-1-(2-phenylethyl)-3-(propen-2-yl)-3-pyrrolidineacetate (1.93 g, 4.99 mmol) in dry CH2Cl2 (20 mL) is treated with diisopropylethylamine (1.04 mL, 5.99 mmol) and 3,4-difluorobenzoyl chloride (691 μL, 5.49 mmol). The solution is allowed to warm to room temperature, stirring under N2 overnight. The solution is diluted with EtOAc (100 mL) and washed with 1N HCl (25 mL), 1N NaOH (25 mL), and brine (25 mL). The organic layer is dried over anhydrous MgSO4, filtered, and concentrated under reduced pressure to give 3.60 g of a brown oil. The oil is purified by silica gel chromatography (50 g SG; 25% EtOAc/hexane) to provide 2.10 g (80%) of the title compound as a yellow, amorphous solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712300
Source datasetuspto-grants-1998_01
ORD IDord-d197421396d0417f91f2c62444f8ee8b
Source noteuspto-grants-1998_01