Diethyl Ether → HCID 86737257, compound

HRID 1032364Notes

Reaction equation

HRID 1032364 reaction equation
[CH2:1]1[CH2:10][O:9][CH2:8][CH:3]([CH2:4][CH2:5][CH:6]=C)[O:2]1.CC[O:13]CC.I([O-])(=O)(=O)=O.[Na+].I([O-])(=O)(=O)=O>[Os](=O)(=O)(=O)=O.O>[CH2:1]1[CH2:10][O:9][CH2:8][CH:3]([CH2:4][CH2:5][CH:6]=[O:13])[O:2]1

Participants

7

Procedure

A mixture of 5-ethylenedioxy-1-hexene (6.0 g.), osmium tetroxide (0.5 g.), ether (150 ml.) and water (150 ml.) is treated portionwise with sodium metaperiodate (19.3 g.) so that the reaction temperature does not exceed 30°. After the addition of the periodate, a voluminous white solid precipitates out. The mixture is stirred 2.5 hrs. at room temperature, then filtered, and the solid portion is washed with more aqueous ether. The aqueous portion of the filtrate is separated and extracted with three portions of methylene chloride. The combined organic phases are dried with magnesium sulfate, filtered, and evaporated in vacuo. Distillation of the residue yields 4-ethylenedioxy-pentanal (65% yield) b.p. 56°-58°/10.5 m nmr (CDCl3) δ: 1.27 (s, CH3), 2.04-2.80 (m, --CH2 --CH2 --); 3.9 (s, --OCH2 --CH2 --O), 9.73 (t, O=C--H). IR (film) μ: 3.66; 3.79.

Workup

  1. customdoes not exceed 30°
  2. customa voluminous white solid precipitates out
  3. filtrationat room temperature, then filtered
  4. washthe solid portion is washed with more aqueous ether
  5. customThe aqueous portion of the filtrate is separated
  6. extractionextracted with three portions of methylene chloride
  7. dry with materialThe combined organic phases are dried with magnesium sulfate
  8. filtrationfiltered
  9. customevaporated in vacuo
  10. distillationDistillation of the residue

Sources & evidence

ORD record
ord-dd8f1a8b272d48b4a87017242ab3f76d
Source dataset
uspto-grants-1990_09
Patent number
US04957912

Reaction notes

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