Potassium Hydroxide → HCID 70385933, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:20]=[CH:19][C:18]2[C@@H:17]3[C@H:8]([C@H:9]4[C@@:13]([CH2:15][C@@H:16]3[O:21]C(=O)C)([CH3:14])[C@@H:12]([O:25]C(=O)C)[CH2:11][CH2:10]4)[CH2:7][C:6](=[O:29])[C:5]=2[CH:4]=1.[OH-].[K+]>CO.O>[CH3:1][O:2][C:3]1[CH:20]=[CH:19][C:18]2[C@@H:17]3[C@H:8]([C@H:9]4[C@@:13]([CH2:15][C@@H:16]3[OH:21])([CH3:14])[C@@H:12]([OH:25])[CH2:11][CH2:10]4)[CH2:7][C:6](=[O:29])[C:5]=2[CH:4]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The keto-diester (23) (21 mg, 0.05 mmole) was added to a degassed 10% solution of potassium hydroxide in methanol-water (19:1) (4 ml), and the solution was boiled for 15 min under nitrogen. The solvent was removed by evaporation under reduced pressure, and the residue was dissolved in ether. The extract was washed in succession with dilute hydrochloric acid and water, dried, and evaporated to give a residue which was chromatographed on silica (1 g) eluted with ether to give the product (6A) (15 mg, 90%), m.p. 225°-6° C. (from ether-light petroleum), νmax 3460 (OH) and 1655 cm-1 (CO), δ (250 MHz) 7.61 (1 H, d, J 2.5 Hz, 4-proton), 7.37 (1 H, d, J 8 Hz, 1-proton), 7.17 (1 H, dd, J 8 and 2.5 Hz, 2-proton), 4.84 (1 H, dt, H 3 and 2.5 Hz, 11-proton), 3.85 (3 H, s, OCH3), 3.74 (1 H, dd, J 9 and 7 Hz, 17-proton) 2.78 (1 H, dd, J 15 and 2.5 Hz, 12-proton), 2.71 (1 H, dd, J 10.5 and 2.5 Hz, 9-proton), 2.44 (10 H, m), 1.04 (3 H, s, 18-CH3);
Workup
- customThe solvent was removed by evaporation under reduced pressure
- dissolutionthe residue was dissolved in ether
- washThe extract was washed in succession with dilute hydrochloric acid and water
- customdried
- customevaporated
- customto give a residue which
- customwas chromatographed on silica (1 g)
- washeluted with ether
Sources & evidence
- ORD record
- ord-5abbc26551c3436e9f98a276eb43ee40
- Source dataset
- uspto-grants-1989_11
- Patent number
- US04882439
Reaction notes
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