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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182763Generated: November 2, 2026

Triethylamine → 7-Bromo-8-chloromethyl-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-one

https://huagongshe.com/reaction/1182763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant7-Bromo-8-hydroxymethyl-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-oneHCID 57671951—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product7-Bromo-8-chloromethyl-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-oneHCID 5767176172.3%

Reaction Steps

7-Bromo-8-hydroxymethyl-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-one (Reference Compound No. 1, 37.5 mg, 0.125 mmol) was dissolved in anhydrous dichloromethane (1 mL), and triethylamine (20.9 μL, 0.150 mmol) and methanesulfonyl chloride (10.7 μL, 0.138 mmol) were added thereto successively. The reaction mixture was stirred at room temperature overnight. Ethyl acetate (10 mL) and water (10 mL) were added to the reaction mixture and partitioned. The organic layer was washed with saturated brine (10 mL), dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (28.7 mg) as an orange amorphous product. (Yield 72%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664221B2
Source datasetuspto-grants-2014_03
ORD IDord-a63b9c60dddb4ba19860b1a098d0a804
Source noteuspto-grants-2014_03