p-Toluenesulfonic acid monohydrate → Butanoic acid, 4-(2-oxocyclopentyl)-, ethyl ester
Reaction equation
[C:1]([CH2:4][CH2:5][CH2:6][CH:7]1[CH2:11][CH2:10][CH2:9][C:8]1=[O:12])([OH:3])=[O:2].O.[C:14]1(C)C=CC(S(O)(=O)=O)=C[CH:15]=1>C(O)C>[C:1]([CH2:4][CH2:5][CH2:6][CH:7]1[CH2:11][CH2:10][CH2:9][C:8]1=[O:12])([O:3][CH2:14][CH3:15])=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In the manner described in Example 3, treatment of 2-(3-carboxypropyl)cyclopentan-1-one (Example 5) with p-toluenesulfonic acid monohydrate in ethanol gives a colorless oil, b.p. 93° C. (0.10 mm).
Workup
- customgives a colorless oil, b.p. 93° C. (0.10 mm)
Sources & evidence
- ORD record
- ord-2b59a033e25e4fd4adefb08677a78c86
- Source dataset
- uspto-grants-1979_12
- Patent number
- US04179574
Reaction notes
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