Trifluoroacetic acid → HCID 68866292, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:10]2[S:11][CH:12]=[CH:13][N:14]=2)O)=[CH:4][C:3]=1[F:15].C(O)(C(F)(F)F)=O.C([SiH](CC)CC)C>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:10]2[S:11][CH:12]=[CH:13][N:14]=2)=[CH:4][C:3]=1[F:15]Participants
4
Procedure
A solution of (4-Bromo-3-fluoro-phenyl)-thiazol-2-yl-methanol (3.4 g, 12.6 mmol), TFA (25 mL), and Triethylsilane (10 mL, 63 mmol), were refluxed overnight. The reaction was then concentrated under vacuum, and purified by silica gel chromatography (gradient elution 10-40% Ethylacetate/Hexanes). Yield 1.96 g, 61%.
Workup
- concentrationThe reaction was then concentrated under vacuum
- custompurified by silica gel chromatography (gradient elution 10-40% Ethylacetate/Hexanes)
Sources & evidence
- ORD record
- ord-620393d39a114a16b9b44aa4dadb04f3
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07473790B2
Reaction notes
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