p-Toluenesulfonic acid monohydrate → HCID 13037859, compound
Reaction equation
[OH2:1].[C:2]1([CH3:12])[CH:7]=[CH:6][C:5](S(O)(=O)=O)=C[CH:3]=1.[O:13]1[CH2:18][CH2:17]OCC1.O>>[OH:13][CH:18]1[CH2:17][C:12](=[O:1])[C:2]([CH2:7][C:6]#[CH:5])=[CH:3]1Participants
Procedure
To a solution of 40.2 g (0.295 mole) of the title compound of Example 1 in 800 ml of a 8:1 dioxane/water mixture was added 4 g (0.021 mole) of p-toluenesulfonic acid monohydrate. The reaction mixture was heated at 83° for 36 hours under argon, cooled, and diluted with 500 ml of ethyl acetate. The organic phase was washed once with water and two times each with 5% sodium bicarbonate solution and brine solution. The aqueous washes were combined and extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered, and concentrated. Chromatography of the combined crude materials on silica gel (using 25% ethyl acetate in hexane as eluent) gave 12.45 g of the intermediate compound 4-hydroxy-5-(2-propynyl)-2-cyclopenten-1-one as a viscous oil. Structure assignment was confirmed by the proton nmr spectrum.
Sources & evidence
- ORD record
- ord-4c88822fc99940ed802efdc88856c5bb
- Source dataset
- uspto-grants-1986_03
- Patent number
- US04578505
Reaction notes
Loading…