Triethylamine → HCID 66759725, compound

HRID 1850404Notes

Reaction equation

HRID 1850404 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

7

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

  1. customsynthesized in Reference Example 45
  2. washThe extract was washed with saturated saline
  3. customdried
  4. concentrationfollowed by concentration under reduced pressure
  5. 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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