HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromohexane → 1,4-Dibromo-2,5-bis(hexyloxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,5-Dibromohydroquinone | HCID 280945 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1,4-Dibromo-2,5-bis(hexyloxy)benzene | HCID 16726204 | — |
Reaction Steps
A suspension of KOH powder (10.47 g, 186.6 mmol) in dried DMSO (360 mL) was degassed under vigorous stirring for 1 h. 2,5-dibromo-1,4-dihydroxybenzene (5 g, 18.66 mol) and 1-bromohexane (5.8 mL, 41.06 mmol) were added and stirred for 12 h. The solution was concentrated and precipitated in water, filtered, washed with methanol. The product was recrystallized in ethanol, dried in vacuo (4.518 g, 55.5%). 1H NMR(300 MHz, CDCl3): δ 7.08 (s, 2H), 3.95 (t, 4H), 1.8 (m, 4H), 1.49 (m, 4H). 1.37 (m, 8H), 0.9 (t, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633140B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-ac65d9e1b72446fe9a359217dd2cf247 |
| Source note | uspto-grants-2014_01 |