Potassium Hydroxide → HCID 70385933, compound

HRID 1639182Notes

Reaction equation

HRID 1639182 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]=1

Participants

4

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

  1. customThe solvent was removed by evaporation under reduced pressure
  2. dissolutionthe residue was dissolved in ether
  3. washThe extract was washed in succession with dilute hydrochloric acid and water
  4. customdried
  5. customevaporated
  6. customto give a residue which
  7. customwas chromatographed on silica (1 g)
  8. washeluted with ether

Sources & evidence

ORD record
ord-5abbc26551c3436e9f98a276eb43ee40
Source dataset
uspto-grants-1989_11
Patent number
US04882439

Reaction notes

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