HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500131Generated: October 31, 2026
6-Bromoquinoline → HCID 67223792, compound
https://huagongshe.com/reaction/500131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Bromoquinoline | HCID 79243 | — |
| Reactant | 2-Bromo-1,1-dimethoxyethane | HCID 81672 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 67223792 | HCID 67223792 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767675B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-655e87f21cc745dd850d0af1d3d939cf |
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| Source note | uspto-grants-2010_08 |
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