Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Monobenzone | HCID 7638 | — |
| Reactant | 1-Bromopentane | HCID 8057 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 67715504 | HCID 67715504 | — |
Reaction Steps
30 g (150 mmol) 4-(benzyloxy)phenol and 22.35 g 1-bromo-pentane (150 mmol) were dissolved in 250 ml acetone. The solution was heated to 80° C. and stirred with a mechanical stirrer. At this temperature, 118.5 g K2CO3 (1.09 mol) was added in one portion. The resulting heterogeneous solution was allowed to stir at 80° C. for 16 hours. The reaction was monitored by TLC until completion. Excess K2CO3 and the byproduct KBr were removed by filtration. The solution was then acidified with concentrated HCl. Evaporation of the solvent resulted in a light yellow colored oil. No further purifications were needed to obtain the 1-pentyloxy-4-(benzyloxy)phenyl ether intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05668614 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-1a1846d0c68446c39f8fc9fe249d32cb |
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| Source note | uspto-grants-1997_09 |
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