Boron trifluoride etherate → 2-allyl-2-phenyltetrahydro-2H-pyran

To a solution of 2-phenyltetrahydro-2H-pyran-2-ol (1.066 g, 5.98 mmol) and allyltrimethylsilane (1.901 mL, 11.96 mmol) in CH2Cl2 (25 mL) at 0° C. was added BF3.OEt2 (0.758 mL, 5.98 mmol) dropwise, and the mixture was stirred at the same temperature for 1 hr. Then the reaction was quenched with saturated NaHCO3 and the product was extracted with EtOAc. The extract was washed with brine, and the combined aqueous layers were back extracted with EtOAc once and combined. The extracts were dried over Na2SO4 and evaporated to give an oily residue. It was purified by Combiflash (80 g silica gel) eluting with 1:9 followed by 4:6 EtOAc-hexane to give 2-allyl-2-phenyltetrahydro-2H-pyran as oil (0.954 g). 1H NMR (400 MHz, CDCl3) δ ppm 7.10-7.45 (5 H, m), 5.47-5.65 (1 H, m, J=17.19, 10.11, 7.33, 7.33 Hz), 4.84-5.00 (2 H, m), 3.64-3.78 (1 H, m), 3.41-3.57 (1 H, m), 2.35-2.48 (1 H, m), 2.20-2.35 (1 H, m), 1.55-1.81 (4 H, m), 1.35-1.54 (2 H, m).

1. customThen the reaction was quenched with saturated NaHCO3
2. extractionthe product was extracted with EtOAc
3. washThe extract was washed with brine
4. extractionthe combined aqueous layers were back extracted with EtOAc once
5. dry with materialThe extracts were dried over Na2SO4
6. customevaporated
7. customto give an oily residue
8. customIt was purified by Combiflash (80 g silica gel)
9. washeluting with 1:9

ORDレコード

ord-c57c96884e504d9586c944a07b1170a6

出典データセット

uspto-grants-2015_11

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09187437B2