Allyl bromide → 13990-72-2

To a solution of 4-fluorophenol (1p) (30 g, 268.0 mmol) in acetone (250 mL), anhydrous K2CO3 (65 g, 468.3 mmol) was added followed by 3-bromo-propene (2p) (28 mL, 321.1 mmol). The resulting mixture was refluxed for 16 hours, cooled to room temperature and then poured onto ice water (500 mL). The aqueous layer was extracted with ether (3×250 mL) and the combined organic layers were washed with 2 M NaOH (2×150 mL) and dried over a mixture of anhydrous K2CO3 and Na2SO4. The solvent was removed under vacuum to afford the desired product (3p) (40.4 g, 99%) as light yellow oil. 1H NMR (400 MHz, CDCl3) δ7.01-6.92 (m, 2H), 6.89-6.82 (m, 2H), 6.10-6.82 (m, 1H), 5.44-5.41 (m, 1H), 5.39-5.37 (m, 1H), 4.51-4.448 (m, 2H).

1. temperatureThe resulting mixture was refluxed for 16 hours
2. additionpoured onto ice water (500 mL)
3. extractionThe aqueous layer was extracted with ether (3×250 mL)
4. washthe combined organic layers were washed with 2 M NaOH (2×150 mL)
5. dry with materialdried over a mixture of anhydrous K2CO3 and Na2SO4
6. customThe solvent was removed under vacuum

ORD record

ord-33f5344f353c422593308726b6008f37

Source dataset

uspto-grants-2010_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07799782B2