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Chemical Structure| 82272-08-0 Chemical Structure| 82272-08-0

Structure of 82272-08-0

Chemical Structure| 82272-08-0

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Product Details of [ 82272-08-0 ]

CAS No. :82272-08-0
Formula : C8H16O2Si
M.W : 172.30
SMILES Code : C[Si](OC1=CCCOC1)(C)C
MDL No. :MFCD27929256

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Application In Synthesis of [ 82272-08-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 82272-08-0 ]

[ 82272-08-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 104-21-2 ]
  • [ 82272-08-0 ]
  • [ 1369628-67-0 ]
YieldReaction ConditionsOperation in experiment
96% With bis(trifluoromethanesulfonyl)amide; In dichloromethane; at 0℃; for 0.166667h;Inert atmosphere; Example 116; (4aR* , 1 OaR* )-8 -methoxy-4a-methyl- 1 ,3 ,4,4a,5 , 1 Oa-hexahydro-5 -spiro benzo g] isochromene-10,4'-oxazoll -2'-amine; Step A:; To a solution of (5,6-dihydro-2H-pyran-3-yloxy)trimethylsilane (50.9 g, 296 mmol, prepared according to the method described in WO 2009/43883) and 4- methoxybenzyl acetate (35.5 g, 197 mmol) in dichloromethane (394 mL, 197 mmol) at 0C under N2 was added dropwise a solution of 1,1,1-trifluoro-N- (trifluoromethylsulfonyl)methanesulfonamide (2.77 g, 9.85 mmol) in DCM (24 mL). The mixture was stirred at 0C for 10 minutes and quenched with ice water (30 mL). The organic layer was separated, washed with brine (50 mL), dried (MgS04) and concentrated in vacuo. The residue isolated was purified by flash chromatography on silica gel (Ready Sep 330 g) eluting with 10% EtOAc/hexane to provide 4-(4-methoxybenzyl)dihydro-2H-pyran-3(4H)-one (41.5 g, 96% yield) as a solid. 1H NMR (400 MHz, CDC13) delta 7.07 (d, J=8.61 Hz, 2H), 6.83 (d, J=8.61 Hz, 2H), 4.06 (d, J=15.65 Hz, 1H), 3.98-3.94 (m, 2H), 3.79 (s, 3H), 3.76-3.70 (m, 1H), 3.29 (dd, Jl=4.30 Hz, J2=14.08 Hz, 1H), 2.71-2.63 (m, 1H), 2.06-1.98 (m, 1H), 1.79-1.69 (m, 1H).
88% A solution of l,l,l-trifluoro-N-(trifluoromethylsulfonyl) methanesulfonamide (0.304 g, 1.08 mmol) in DCM (5 mL) was added dropwise to a solution of (5,6-dihydro-2H-pyran-3-yloxy)trimethylsilane (19.5 g, 110 mmol, prepared according to the method described in WO 2009/043883) and <strong>[104-21-2]4-methoxybenzyl acetate</strong> (19.5 g, 108 mmol) in dichloromethane (216 mL, 108 mmol) at 0C under N2 atmosphere. The mixture was stirred at 0C for 10 minutes and quenched with ice water (30 mL). The organic layer was separated, washed with brine (50 mL), dried (MgS04) and concentrated in vacuo. The crude isolated was purified by flash chromatography on silica gel (Ready Sep 220 g) eluting with 10% EtOAc/hexane to provide 4-(4-methoxybenzyl)dihydro-2H-pyran-3(4H)-one (21 g, 88% yield) as a solid. 1H NMR (400 MHz, CDC13) delta 7.07 (d, J=8.61 Hz, 2H), 6.83 (d, J=8.61 Hz, 2H), 4.06 (d, J=15.65 Hz, 1H), 3.98-3.94 (m, 2H), 3.79 (s, 3H), 3.76-3.70 (m, 1H), 3.29 (dd, Jl=4.30 Hz, J2=14.08 Hz, 1H), 2.71-2.63 (m, 1H), 2.06-1.98 (m, 1H), 1.79-1.69 (m, 1H).
 

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