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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295981Generated: October 31, 2026

Toluene → HCID 67136588, compound

https://huagongshe.com/reaction/1295981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantIodoethaneHCID 6340—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 67137822HCID 67137822—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
ProductHCID 67136588HCID 6713658873%

Reaction Steps

Tetra-n-butylammonium bromide (380 mg, 1.18 mmol) and ethyl iodide (0.4 ml, 5.0 mmol) were added to a solution of 1-{3-(tert-butyl)-5-[(3S,4S)-3-hydroxy-4-(methoxymethoxy)tetrahydro-1H-1-pyrrolyl]-4-methoxyphenyl}-1-ethanone (830 mg, 2.36 mmol) in a toluene (5 ml) −50% aqueous NaOH (5 ml) mixed solvent at room temperature in that order and the mixture was stirred for 19 hours. After further adding ethyl iodide (0.2 ml) and stirring for 9 hours, more ethyl iodide (0.2 ml) was added and stirring was continued for 60 hours. The mixture was diluted with water, extraction was performed with ethyl acetate and the extract was washed with brine. After drying with anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (650 mg, 73%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-f7bb3cf36969457f98076c09529d9fcd
Source noteuspto-grants-2007_07