Ammonium Chloride → Benzo(b)thiophene-3-ol

HRID 2172123Notes

Reaction equation

HRID 2172123 reaction equation
[CH3:1][S:2][C:3]1[CH:12]=[CH:11][CH:10]=[CH:9][C:4]=1[C:5](OC)=[O:6].[Li+].CC([N-]C(C)C)C.[Cl-].[NH4+]>C1COCC1>[S:2]1[CH:1]=[C:5]([OH:6])[C:4]2[CH:9]=[CH:10][CH:11]=[CH:12][C:3]1=2

Participants

5

Conditions

Temperature
-78 °C

Procedure

A solution of methyl 2-(methylthio)benzoate (4.0 g, 22.00 mmol) in THF (60 mL) was added to a solution of freshly prepared LDA (2M in THF, 17.5 mL, 35 mmol) placed at −78° C. The reaction mixture was stirred for 1 hour at −78° C., then overnight at room temperature. The reaction mixture was diluted by addition of a saturated solution of ammonium chloride (50 mL). The aqueous phase was separated and extracted with ethyl acetate (3×70 mL). The combined organic phases were washed with a saturated solution of sodium chloride (40 mL), dried over sodium sulfate, filtered and concentrated to dryness. The residue was purified by chromatography on silica gel using petroleum ether/ethyl acetate (95:5 to 9:1) as eluent. The title product was obtained as a pink solid (1.74 g, 53%).

Workup

  1. customplaced at −78° C
  2. customovernight
  3. customat room temperature
  4. customThe aqueous phase was separated
  5. extractionextracted with ethyl acetate (3×70 mL)
  6. washThe combined organic phases were washed with a saturated solution of sodium chloride (40 mL)
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated to dryness
  10. customThe residue was purified by chromatography on silica gel

Sources & evidence

ORD record
ord-da8c97b41136492aa73d67dd7b3a28b1
Source dataset
uspto-grants-2015_06
Patent number
US09051321B2

Reaction notes

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