HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(4-Phenylphenoxy)-1-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | 3-Bromo-1-propanol | HCID 12308 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Phenylphenoxy)-1-propanol | HCID 28351739 | 43% |
Reaction Steps
Into a 200 ml flask, 7.82 g (41.1 mmol) of 4-hydroxybiphenyl, 83 ml of ethanol, 6 g (43.2 mmol) of 3-bromo-1-propanol and a NaOH aqueous solution (1.73 g (43.2 mmol) of NaOH/6 ml of water) were sequentially added, and the mixture was heated and refluxed for 6.5 hours. To the reaction solution, 50 ml of water was added, whereupon precipitated crystals were collected by filtration and recrystallized from ethanol to obtain 4.0 g (yield: 43%) of 4-(3-hydroxypropoxy)biphenyl (1) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05861534 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-9e0ab87c47fd417cb1c3eb6c78e3154c |
| Source note | uspto-grants-1999_01 |