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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715924Generated: October 30, 2026

Ammonium Chloride → tert-Butyl N-[(3S)-1-(4-bromo-3-methylphenyl)-5-oxopyrrolidin-3-yl]carbamate

https://huagongshe.com/reaction/715924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantCesium fluorideHCID 25953—
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant2-Bromo-5-iodotolueneHCID 2735574—
Reactant(S)-tert-Butyl (5-oxopyrrolidin-3-yl)carbamateHCID 45091936—
CatalystCopper iodideHCID 83717—
SolventAcetonitrileHCID 6342—
Producttert-Butyl N-[(3S)-1-(4-bromo-3-methylphenyl)-5-oxopyrrolidin-3-yl]carbamateHCID 11789347696.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 2-bromo-5-iodotoluene (1.5 g), tert-butyl ((S)-5-oxopyrrolidin-3-yl)carbamate (2.7 g), copper iodide (95 mg), cesium fluoride (1.9 g), and N,N-dimethylethylenediamine (0.11 ml) in acetonitrile (20 ml) was stirred at 100° C. for 3 hours under a nitrogen atmosphere. After cooling, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. The extract was washed with a 10% aqueous sodium thiosulfate solution and saturated saline in this order and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform-methanol) to obtain the title compound (1.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187489B2
Source datasetuspto-grants-2015_11
ORD IDord-33b112249b754d16a700070604b8e3d4
Source noteuspto-grants-2015_11