Allylchlorodimethylsilane → tert-butyl-N-{4-[allyl(dimethyl)silyl]-2-methoxyphenyl}carbamate

Temperature

-78 °C

To 2.4 g (20.6 mmol, 1.2 eq) of 35% potassium hydride suspended in 70 ml of anhydrous THF under an argon atmosphere, at room temperature 5.2 g (17.2 mmol) of tert-butyl-N-(4-bromo-2-methoxyphenyl)carbamate 4 diluted in 60 ml of anhydrous THF is added dropwise. This mixture is shaken for 10 min before cooling to −78° C. When this temperature is reached, 23.5 ml (35.3 mmol, 2.05 eq) of 1.5 M tert-butyllithium is added through a cannula in hexane diluted in 50 ml of anhydrous THF and previously cooled to −78° C. The reaction is allowed to progress for 20 min at −78° C. before adding 6.2 ml (41.3 mmol, 2.4 eq) of allyl(chloro)dimethylsilane all at once. The temperature is allowed to rise to −10° C. then the medium is hydrolyzed with a small amount of water. Next, 90 ml of AcOEt is added and the organic phase is washed with H2O (3×90 ml), 1 M NaHSO4 (2×90 ml), then a saturated aqueous solution of NaCl (1×90 ml), and lastly, dried on MgSO4. Concentration under vacuum gives an orange oil which is purified by column chromatography (eluent petroleum ether/AcOEt 9:1), producing 4.28 g of a colorless oil (yield: 77%).

1. additionis added dropwise
2. temperaturepreviously cooled to −78° C
3. waitto progress for 20 min at −78° C.
4. customto rise to −10° C.
5. washthe organic phase is washed with H2O (3×90 ml), 1 M NaHSO4 (2×90 ml)
6. dry with materiala saturated aqueous solution of NaCl (1×90 ml), and lastly, dried on MgSO4
7. concentrationConcentration under vacuum
8. customgives an orange oil which
9. customis purified by column chromatography (eluent petroleum ether/AcOEt 9:1)

ORD record

ord-c0d11dbd4a154a38b4c69cb2e5952676

Source dataset

uspto-grants-2007_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07238693B2