Hexane → 1-(2,2-Diethoxyethoxy)-4-fluorobenzene

A solution of p-fluorophenol (28.1 g., 0.25 mole) in DMF (30 ml.) is added dropwise to a suspension of hexane (2 × 30 ml.)-prewashed sodium hydride (50% oil dispersion, 12.5 g., 0.26 mole) in DMF (120 ml.). The resulting mixture is stirred at room temperature for 10 minutes, treated with bromoacetaldehyde diethyl acetal (49.3 g., 0.25 mole) and finally heated on a steam bath for 4 hours. The reaction mixture is allowed to come to room temperature and the precipitated sodium bromide is filtered off. DMF is then removed on a rotary evaporator, the oil residue is diluted with acetone (100 ml.) and another quantity of sodium bromide is precipitated which again is removed by filtration. The filtrate is then concentrated on a rotary evaporator leaving an oil residue which is vacuum distilled at 87°/0.05 mm to yield the desired product as colorless oil (46.7 g., 0.205 mole, 82%). Ir (neat) 3.4~3.5, 6.21, 6.64, 8.00, 8.25, 8.83, 9.32, 12.08, 13.20μ; pmr (CCl4) δ 1.17 (6H, t J=7.5Hz), 3.57 (2H, q, J=7.5 Hz), 3.61 (2H, q, J=7.5 Hz), 3.85 (2H, d, J=5Hz), 4.68 (1H, t, J=5Hz), 6.6-7.1 (4H, m).

1. temperaturefinally heated on a steam bath for 4 hours
2. customto come to room temperature
3. filtrationthe precipitated sodium bromide is filtered off
4. customDMF is then removed on a rotary evaporator
5. additionthe oil residue is diluted with acetone (100 ml.)
6. customanother quantity of sodium bromide is precipitated which
7. customagain is removed by filtration
8. concentrationThe filtrate is then concentrated on a rotary evaporator
9. customleaving an oil residue which
10. distillationdistilled at 87°/0.05 mm

ORD record

ord-862fe6a0505a4634a7ea6a95c58c5978

Source dataset

uspto-grants-1977_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04061643