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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257791Generated: November 3, 2026

6-Bromoquinoline → HCID 67223792, compound

https://huagongshe.com/reaction/1257791

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-BromoquinolineHCID 79243—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
ReactantSodium methanethiolateHCID 4378561—
SolventEthanolHCID 702—
SolventDimethylacetamideHCID 31374—
ProductHCID 67223792HCID 67223792—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 6-bromoquinoline (0.832 g, 4.0 mmol) in N,N-dimethylacetamide (4.0 mL) was added sodium methyl mercaptide (0.841 g, 12.0 mmol). The reaction mixture was heated at 150° C. for 2 h. After cooling, 2-bromo-1,1-dimethoxyethane (1.41 mL, 12.0 mol) was then added, and the reaction mixture was diluted with ethanol (5 mL), and heated at 80° C. for 1 h. After the precipitated salt was isolated by filtration, the mother liquor was evaporated under reduced pressure. The residue was diluted with diethyl ether (50 mL), washed with water, brine, dried over sodium sulfate, filtered, and concentrated. The residue was directly used in the next reaction step without further purification. LCMS: (M+H)=249.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461330B2
Source datasetuspto-grants-2013_06
ORD IDord-c1feb3ba823041c4a90692de66654605
Source noteuspto-grants-2013_06