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TCI Practical Example: Hosomi-Sakurai Allylation via an Imine Intermediate

We are proud to present the three component reaction with the Hosomi-Sakurai allylation reaction using allyl(trimethyl)silane.

TCI Practical Example: Hosomi-Sakurai Allylation via an Imine Intermediate

Used Chemicals

Procedure

Cyclopentanone (890 µL, 10 mmol), benzyl carbamate (1.81 g, 12 mmol) and allyltrimethylsilane (2.2 mL, 14 mmol) were dissolved in dichloromethane (14 mL). After cooling to 0 °C, BF3·Et2O (1.51 mL, 12 mmol) was added and the reaction mixture was stirred for 21 hours at room temperature. After the reaction, the mixture was washed with satd. NaHCO3 aq. (10 mL), brine (20 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (hexane:ethyl acetate = 9:1) to afford benzyl (1-allylcyclopentyl)carbamate (1.84 g, 71% yield) as a clear yellow liquid.

Experimenter’s Comments

The reaction solution was monitored by UPLC.

Analytical Data

Benzyl (1-Allylcyclopentyl)carbamate

1H NMR (400 MHz, CDCl3); δ 7.35-7.29 (m, 5H), 5.82-5.72 (m, 1H), 5.06-5.02 (m, 4H), 4.68 (brs, 1H), 2.52-2.51 (m, 2H), 1.76-1.61 (m, 8H).

Other References

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