Ammonium Chloride → Benzo(b)thiophene-3-ol
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=2Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- customplaced at −78° C
- customovernight
- customat room temperature
- customThe aqueous phase was separated
- extractionextracted with ethyl acetate (3×70 mL)
- washThe combined organic phases were washed with a saturated solution of sodium chloride (40 mL)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated to dryness
- customThe residue was purified by chromatography on silica gel
Sources & evidence
- ORD record
- ord-1624e469561449cc82160ad668b8b8f2
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08846711B2
Reaction notes
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