HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626807Generated: November 1, 2026
1,4-Dibromobenzene → HCID 68193231, compound
https://huagongshe.com/reaction/1626807
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobenzene | HCID 7804 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 45867410 | HCID 45867410 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68193231 | HCID 68193231 | 69% |
Reaction Steps
1,4-Dibromobenzene (6.5 g, 27 mmol) was dissolved in tetrahydrofuran (120 mL), and a solution of n-butyllithium in hexane (2.6 M, 10 mL, 27 mmol) was added at −78° C., followed by stirring at the same temperature for 30 minutes. A solution of N,6-dimethoxy-N-methylnicotinamide (2.7 g, 14 mmol) in tetrahydrofuran (20 mL) was added to the reaction solution, followed by stirring at −78° C. for further 30 minutes. Water was added to the reaction solution, followed by extraction with ethyl acetate, and subsequently the organic layer was concentrated under reduced pressure. The resulting residue was purified by chromatography on a silica gel column (Moritex Corporation, elution solvent: hexane/ethyl acetate), and a fraction corresponding to the Rf value=0.50 (hexane/ethyl acetate=10/1) by thin layer chromatography was concentrated under reduced pressure to afford the title compound (2.8 g, 9.4 mmol) as a white solid (yield 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785462B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-0f5c82a0e6a8470cb865e8db4319fb3f |
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| Source note | uspto-grants-2014_07 |
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