HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzylphenol → HCID 67860114, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzylphenol | HCID 7563 | — |
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67860114 | HCID 67860114 | 164.2% |
Reaction Steps
To a suspension of sodium hydride (60%, 2.0 g, 49 mmol) in dimethylformamide (200 mL) was added 4-benzylphenol (6.0 g, 33 mmol) portionwise. The mixture was stirred at room temperature for 2 hours, then 1-bromo-3-chloropropane (5.1 mL, 49 mmol) was added and the mixture was stirred at room temperature overnight. The reaction was quenched with methanol (10 mL) and filtered through Celite®. The filtrate was taken up in ether (300 mL), washed thrice with water (150 mL) and dried over sodium sulfate. The solution was concentrated to give 7.5 g (79%) of 4-chloropropoxyphenyl-1-phenyl-methane methane as an amber oil. 1H NMR (CDCl3): δ7.44-6.78 (m,9H), 4.01(t,2H), 3.99(s,2H), 3.55(t,2H), 1.98(m,4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05192786 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-996db55d9c4943289c5be9dcb2392c92 |
| Source note | uspto-grants-1993_03 |