HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875246Generated: October 29, 2026
1-Bromopentane → 4-Bromo-4'-(pentyloxy)-1,1'-biphenyl
https://huagongshe.com/reaction/875246
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromopentane | HCID 8057 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-4'-hydroxybiphenyl | HCID 95093 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Bromo-4'-(pentyloxy)-1,1'-biphenyl | HCID 2801388 | 53% |
Reaction Steps
Under an argon atmosphere, 4-bromo-4′-hydroxybiphenyl (3.0 g, 12 mmol), 1-bromopentane (3.6 g, 24 mmol), and potassium carbonate (1.66 g, 12 mmol) were dissolved in acetone (60 mL) and stirred under a reflux condition for 24 hours. After they reacted with each other, liquid separation and extraction were performed with water and chloroform. After an organic layer was dried with anhydrous sodium sulfate and filtered, the solvent was distilled off under a reduced pressure. After the obtained reaction mixture was separated and purified with a silica gel column chromatography using chloroform as a moving bed, the mixture was purified by a recrystallization method using chloroform and hexane. Thereby, a white solid of 4-Bromo-4′-pentyloxybiphenyl (A1) was obtained (1.99 g, yield: 53%). The obtained product (A1) was identified by using a 1H-NMR method. 1H-NMR (CDCl3, 400 MHz) δ=7.53-7.51 (d, 2H), 7.48-7.46 (d, 2H), 7.42-7.40 (d, 2H), 7.00-6.95 (d, 2H), 4.01-3.98 (t, 2H), 1.81 (m, 2H), 1.42 (m, 4H), and 0.94 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08981120B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-6f320b01a5d04479971267ff11fdb753 |
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| Source note | uspto-grants-2015_03 |
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