Tetrabutylammonium Fluoride → HCID 71293490, compound

HRID 2362302Notes

Reaction equation

HRID 2362302 reaction equation
[CH3:1][O:2][C:3]([C:5]1[CH:10]([C:11]2[CH:16]=[CH:15][C:14]([C:17]#[N:18])=[CH:13][CH:12]=2)[N:9]2[C:19](=[O:39])[N:20]([CH2:22][CH2:23][CH2:24][S:25]([CH2:28][CH2:29][CH2:30][O:31][Si](C(C)(C)C)(C)C)(=[O:27])=[O:26])[N:21]=[C:8]2[N:7]([C:40]2[CH:45]=[CH:44][CH:43]=[C:42]([C:46]([F:49])([F:48])[F:47])[CH:41]=2)[C:6]=1[CH3:50])=[O:4].CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1>[CH3:1][O:2][C:3]([C:5]1[CH:10]([C:11]2[CH:12]=[CH:13][C:14]([C:17]#[N:18])=[CH:15][CH:16]=2)[N:9]2[C:19](=[O:39])[N:20]([CH2:22][CH2:23][CH2:24][S:25]([CH2:28][CH2:29][CH2:30][OH:31])(=[O:26])=[O:27])[N:21]=[C:8]2[N:7]([C:40]2[CH:45]=[CH:44][CH:43]=[C:42]([C:46]([F:48])([F:47])[F:49])[CH:41]=2)[C:6]=1[CH3:50])=[O:4]

Participants

4

Procedure

Intermediate 21 (282 mg, 0.38 mmol) was dissolved in THF (3 mL), and then a solution of 1 M TBAF in THF (760 μl, 0.76 mmol) was added. The reaction mixture was stirred at RT for 4 hours and then partitioned between EtOAc and water. The organic layer was separated, and the aqueous layer further extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4) and evaporated in vacuo. The resulting residue was purified by silica gel chromatography eluting with a gradient of 0-2% methanol in EtOAc to afford the title compound (89 mg).

Workup

  1. custompartitioned between EtOAc and water
  2. customThe organic layer was separated
  3. extractionthe aqueous layer further extracted with EtOAc
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried (Na2SO4)
  6. customevaporated in vacuo
  7. customThe resulting residue was purified by silica gel chromatography
  8. washeluting with a gradient of 0-2% methanol in EtOAc

Sources & evidence

ORD record
ord-7f85816bdcca4684a1e958494d937384
Source dataset
uspto-grants-2014_04
Patent number
US08691826B2

Reaction notes

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