HCID 18594629, compound → HCID 18594628, compound

HRID 1580213Notes

Reaction equation

HRID 1580213 reaction equation
[CH2:1]1[CH2:28][O:27][C:3]2([CH2:17][CH2:16][C@H:15]([CH2:18][CH2:19][C@@H:20]([OH:26])[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[C@H:4]2[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12])[O:2]1>C(Cl)Cl>[CH2:28]1[CH2:1][O:2][C:3]2([CH2:17][CH2:16][C@H:15]([CH2:18][CH2:19][C:20](=[O:26])[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[C@H:4]2[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12])[O:27]1

Participants

3

Procedure

To a mixture of 14.5 g. of chromium trioxide-pyridine complex in 110 ml. of dry methylene chloride is added with stirring 4.82 g. of 1-methyl 9,9-(ethylenedioxy)-15(S)-hydroxy-prostanoate (Example 134) in 17 ml. of methylene chloride. The resulting dark brown mixture is stirred at ambient temperature for 18 hours. The mixture is filtered and the mother liquor is taken to dryness. The residue is taken up in ether and washed successively with ice cold 5% sodium hydroxide, saturated sodium chloride solution, 30% sodium phosphate monobasic solution and water dried with anhydrous sodium sulfate and evaporated to dryness under reduced pressure to afford 4.17 g. (98%) of product as an oil; λ max 5.71, 5.82μ (carbonyl groups).

Workup

  1. additionTo a mixture of 14.5 g
  2. stirringThe resulting dark brown mixture is stirred at ambient temperature for 18 hours
  3. filtrationThe mixture is filtered
  4. washwashed successively with ice cold 5% sodium hydroxide, saturated sodium chloride solution, 30% sodium phosphate monobasic solution and water
  5. dry with materialdried with anhydrous sodium sulfate
  6. customevaporated to dryness under reduced pressure
  7. customto afford 4.17 g

Sources & evidence

ORD record
ord-896110cec8024790a24601afdfc41168
Source dataset
uspto-grants-1976_01
Patent number
US03932463

Reaction notes

Loading…