Acetic Acid → 6-Bromo-1,2,3,4-tetrahydrocarbazole
Reaction equation
Cl.[Br:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9]N)=[CH:5][CH:4]=1.[C:11](O)(=O)[CH3:12].C(=O)(O)[O-].[Na+]>C1(=O)CCCCC1>[Br:2][C:3]1[CH:8]=[C:7]2[C:6](=[CH:5][CH:4]=1)[NH:9][C:12]1[CH2:11][CH2:5][CH2:4][CH2:3][C:8]2=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Cyclohexanone (1.16 mL, 11.2 mmol) and 4-bromo-phenylhydrazine hydrochloride (2.50 g, 11.2 mmol) were refluxed in cyclohexanone (18 mL) and acetic acid (AcOH) (12 L) for 24 h. The reaction mixture was treated with saturated sodium bicarbonate (Na2CO3) and extracted with ethyl acetate, dried (Na2CO3) and concentrated. The product was purified by column chromatography, giving 479 mg of compound 30 as a solid.
Workup
- extractionextracted with ethyl acetate
- dry with materialdried (Na2CO3)
- concentrationconcentrated
- customThe product was purified by column chromatography
Sources & evidence
- ORD record
- ord-02a059cee42140d5a02850b8679f5981
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08431538B2
Reaction notes
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