Water → 2-(3-bromopropyl)-1,3-dioxolane

HRID 1031648Notes

Reaction equation

HRID 1031648 reaction equation
[H-].C([Al+]C[CH:8]([CH3:10])[CH3:9])C(C)C.[Br:11][CH:12](CC)C(O)=O.[CH:18]([OH:21])([CH3:20])C.[OH2:22]>C1(C)C=CC=CC=1>[Br:11][CH2:12][CH2:10][CH2:8][CH:9]1[O:21][CH2:18][CH2:20][O:22]1

Participants

6

Conditions

Temperature
-70 °C

Procedure

At -70° C., 50 ml of a 1.2-molar solution of diisobutyl aluminum hydride in toluene is added dropwise gradually to a solution of 9.6 g of the ethyl ester of bromobutyric acid in 595 ml of toluene; the mixture is stirred for 15 minutes at -70° C. and then combined dropwise with 10 ml of isopropyl alcohol and 25 ml of water. The mixture is agitated for 2 hours at room temperature, filtered, the filtrate dried with magnesium sulfate and evaporated under vacuum at 25° C. The residue is dissolved in 500 ml of toluene, 10 ml of ethylene glycol and 100 mg of p-toluenesulfonic acid are added, and the mixture is refluxed for 6 hours with the use of a water trap. Subsequently the mixture is diluted with 500 ml of ether, shaken once with a 5% sodium bicarbonate solution and three times with water, the organic extract is dried with magnesium sulfate and concentrated under vacuum at 30° C. Distillation of the residue at 0.6 torr and 43°-45° C. yields 6.8 g of 2-(3-bromopropyl)-1,3-dioxolane as a colorless liquid.

Workup

  1. stirringThe mixture is agitated for 2 hours at room temperature
  2. filtrationfiltered
  3. dry with materialthe filtrate dried with magnesium sulfate
  4. customevaporated under vacuum at 25° C
  5. dissolutionThe residue is dissolved in 500 ml of toluene
  6. addition10 ml of ethylene glycol and 100 mg of p-toluenesulfonic acid are added
  7. temperaturethe mixture is refluxed for 6 hours with the use of a water trap
  8. additionSubsequently the mixture is diluted with 500 ml of ether
  9. stirringshaken once with a 5% sodium bicarbonate solution and three times with water
  10. extractionthe organic extract
  11. dry with materialis dried with magnesium sulfate
  12. concentrationconcentrated under vacuum at 30° C
  13. distillationDistillation of the residue at 0.6 torr and 43°-45° C.

Sources & evidence

ORD record
ord-1e70f09704d546c8a4052cae84ebb6f4
Source dataset
uspto-grants-1990_09
Patent number
US04954524

Reaction notes

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