Triethylamine → HCID 66759725, compound
Reaction equation
C(N(CC)CC)C.FC(F)(F)S([O:13][Si:14]([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15])(=O)=O.[Br:23][C:24]1[C:25]([CH3:36])=[C:26]([CH3:35])[C:27]2[O:31][CH2:30][C:29](=O)[C:28]=2[C:33]=1[CH3:34].O.C(=O)(O)[O-].[Na+]>C(OCC)(=O)C.C1(C)C=CC=CC=1>[Br:23][C:24]1[C:25]([CH3:36])=[C:26]([CH3:35])[C:27]2[O:31][CH:30]=[C:29]([O:13][Si:14]([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15])[C:28]=2[C:33]=1[CH3:34]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
Triethylamine (2.15 g, 21.2 mmol) and tert-butyldimethylsilyl trifluoromethanesulfonate (4.68 g, 17.7 mmol) were sequentially added to a solution of toluene (100 mL) containing 5-bromo-4,6,7-trimethyl-1-benzofuran-3(2H)-one (3.00 g, 11.8 mmol) synthesized in Reference Example 45, and the mixture was stirred at room temperature for 1 hour. The resulting mixture was poured into saturated sodium bicarbonate water, and extraction was performed using ethyl acetate. The extract was washed with saturated saline, and dried using anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was purified by silica gel chromatography (hexane-ethyl acetate 99:1 to 94/6) to give 4.14 g of the title compound (yield: 95%).
Workup
- customsynthesized in Reference Example 45
- washThe extract was washed with saturated saline
- customdried
- concentrationfollowed by concentration under reduced pressure
- customThe residue was purified by silica gel chromatography (hexane-ethyl acetate 99:1 to 94/6)
Sources & evidence
- ORD record
- ord-6f150377ecb94e5896f8e7aad1a786c5
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957069B2
Reaction notes
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