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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295982Generated: October 30, 2026

Triethylamine → HCID 86601498, compound

https://huagongshe.com/reaction/1295982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 67136588HCID 67136588—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86601498HCID 86601498101.4%

Reaction Steps

Triethylamine (0.52 ml, 3.7 mmol) and tert-butyl dimethylsilyltrifluoromethanesulfonate (0.51 ml, 2.2 mmol) were added dropwise in that order to a solution of 1-{3-(tert-butyl)-5-[(3S,4S)-3-ethoxy-4-(methoxymethoxy)tetrahydro-1H-1-pyrrolyl]-4-methoxyphenyl}-1-ethanone (650 mg, 1.71 mmol) in tetrahydrofuran (7 ml) while cooling on ice, and the mixture was stirred at the same temperature for 25 minutes. N-bromosuccinimide (427 mg, 2.40 mmol) was then added and stirring was continued at the same temperature for 25 minutes. After completion of the reaction, the reaction mixture was diluted with saturated aqueous sodium hydrogencarbonate and ethyl acetate and the organic layer was separated. The organic layer was washed with brine and then dried over anhydrous magnesium sulfate. The residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (795 mg, 100%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-6724badd583843cfa0c00651160f8d0b
Source noteuspto-grants-2007_07