HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628207Generated: October 30, 2026
1,4-Dibromobenzene → HCID 13328634, compound
https://huagongshe.com/reaction/628207
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dibromobenzene | HCID 7804 | — |
| Reactant | 2-Hexanone | HCID 11583 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13328634 | HCID 13328634 | 91.5% |
Reaction Steps
n-BuLi (2.5 M in hexanes, 17.0 mL, 42.5 mmol) was added dropwise to a solution of 1,4-dibromobenzene (10.04 g, 42.5 mmol) in THF (100 mL) at −78° C. under nitrogen. After stirring at −78° C. for 1 hour, 2-hexanone (4.5 g, 44.9 mmol) was added dropwise, and the solution was warmed to room temperature and stirred overnight. The reaction mixture was quenched with water and the organic layer was separated. Next, the organic phase was washed with water, dried over Na2SO4, and concentrated on a rotary evaporator to give a crude oil. The crude was purified by column chromatography (silica gel, chloroform) to give 6 as a colorless oil (10.0 g, 91% yield). 1H NMR (500 MHz, CDCl3) δ 7.45 (d, J=8.8 Hz, 2H), 7.30 (d, J=8.8 Hz, 2H), 1.79-1.75 (m, 2H), 1.68 (s, 1H), 1.54 (s, 3H), 1.24-1.28 (m, 4H), 0.85 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09312501B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-8ed7c348c1034c0bafb3a51ce9ff7dce |
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| Source note | uspto-grants-2016_04 |
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