Hexane → (4-Methoxybenzo[b]thiophen-2-yl)boronic acid

HRID 454800Notes

Reaction equation

HRID 454800 reaction equation
CCCCCC.C([Li])CCC.[CH3:12][O:13][C:14]1[C:19]2[CH:20]=[CH:21][S:22][C:18]=2[CH:17]=[CH:16][CH:15]=1.C([O:26][B:27](OC(C)C)[O:28]C(C)C)(C)C>O1CCCC1>[CH3:12][O:13][C:14]1[C:19]2[CH:20]=[C:21]([B:27]([OH:28])[OH:26])[S:22][C:18]=2[CH:17]=[CH:16][CH:15]=1

Participants

6

Procedure

2.5 M Hexane solution of normal butyl lithium (1.07 mL, 2.67 mmol) was slowly added under nitrogen to the 4-methoxybenzothiophene (92a, 368 mg, 2.24 mmol) obtained in Preparation Example 1 dissolved in an anhydrous tetrahydrofuran solution at −78° C., and the reaction mixture was stirred for 30 minutes. To the reaction mixture was slowly added a triisopropylborate solution (i-PrO)3B) (0.55 mL, 2.69 mmol) at room temperature, stirred for one hour, and the reaction was terminated by adding a solution of 2N hydrochloride. The resulting product was extracted with ethyl acetate, evaporated after a treatment with sodium sulfate, and concentrated under reduced pressure, recrystallized and filtered using hexane and ethyl acetate to give the target product 4-methoxybenzothiophene-2-boronic acid (95a, 289 mg, 62%).

Workup

  1. customobtained in Preparation Example 1
  2. stirringstirred for one hour
  3. customthe reaction was terminated
  4. additionby adding a solution of 2N hydrochloride
  5. extractionThe resulting product was extracted with ethyl acetate
  6. customevaporated after a treatment with sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customrecrystallized
  9. filtrationfiltered

Sources & evidence

ORD record
ord-f97016c17fae45b1aca59c4782f79a48
Source dataset
uspto-grants-2013_07
Patent number
US08497260B2

Reaction notes

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