Triethylsilane → 3-Bromo-(5-ethyl-2-thienylmethyl)benzene

HRID 1625768Notes

Reaction equation

HRID 1625768 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]([C:10]2[S:11][C:12]([CH2:15][CH3:16])=[CH:13][CH:14]=2)O)[CH:5]=[CH:6][CH:7]=1.C([SiH](CC)CC)C.C(=O)([O-])O.[Na+]>ClCCl>[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][C:10]2[S:11][C:12]([CH2:15][CH3:16])=[CH:13][CH:14]=2)[CH:5]=[CH:6][CH:7]=1

Participants

5

Conditions

Temperature
-78 °C

Procedure

The above 3-bromophenyl-5-ethyl-2-thienylmethanol (2.90 g) was dissolved in dichloromethane (38 ml), and the mixture was cooled to −78° C. under argon atmosphere. To the mixture were added triethylsilane (6.18 ml) and boron trifluoride diethyl ether complex (2.45 ml), and the mixture was gradually warmed to room temperature over a period of one hour. The mixture was basified with a saturated aqueous sodium hydrogen carbonate solution, and the dichloromethane layer was collected, dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane) to give the desired 3-bromo-(5-ethyl-2-thienylmethyl)benzene (2.57 g) as a colorless syrup. APCI-Mass m/Z 281/283 (M+H).

Workup

  1. temperaturethe mixture was gradually warmed to room temperature over a period of one hour
  2. customthe dichloromethane layer was collected
  3. dry with materialdried over magnesium sulfate
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (hexane)

Sources & evidence

ORD record
ord-454deec6463c4a85bb1ea1c4960b92fb
Source dataset
uspto-grants-2014_07
Patent number
US08785403B2

Reaction notes

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