p-Toluenesulfonic acid → 7-(1-pyrrolyl)-1H-indene
Reaction equation
[N:1]1([C:6]2[CH:14]=[CH:13][CH:12]=[C:11]3[C:7]=2[CH2:8][CH2:9][CH:10]3O)[CH:5]=[CH:4][CH:3]=[CH:2]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[N:1]1([C:6]2[CH:14]=[CH:13][CH:12]=[C:11]3[C:7]=2[CH2:8][CH:9]=[CH:10]3)[CH:2]=[CH:3][CH:4]=[CH:5]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In the manner of Example 1, step I, heating 2.3 g (0.011 mole) of 4-(1-pyrrolyl)-1-indanol in the presence of 0.1 g of p-toluenesulfonic acid and 50 mL of toluene gave 2.0 g of 7-(1-pyrrolyl)-1H-indene as an oil.
Sources & evidence
- ORD record
- ord-e81654d3fe304cfd968954fc91688d8c
- Source dataset
- uspto-grants-1984_04
- Patent number
- US04442296
Reaction notes
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