Acetone → 20880-92-6

HRID 273907Notes

Reaction equation

HRID 273907 reaction equation
[CH3:1][C:2]([CH3:4])=[O:3].S(=O)(=O)(O)O.[OH:10][CH2:11][C:12]([C@H:14]([C@@H:16]([C@@H:18]([CH2:20][OH:21])O)[OH:17])[OH:15])=[O:13].[OH-].[Na+].CO[C:26](C)([CH3:28])[CH3:27]>CCCCCC.C(O)(C)C>[CH3:1][C:2]1([CH3:4])[O:17][C@@H:16]2[C@@H:18]([CH2:20][O:21][C@@:12]3([CH2:11][OH:10])[O:13][C:26]([CH3:28])([CH3:27])[O:15][C@H:14]32)[O:3]1

Participants

8

Conditions

Temperature
5 °C

Procedure

Under nitrogen, acetone (144.0 L, 113.0 kg, 1946 mol) was cooled to 0°-10° C. With stirring, concentrated sulfuric acid (7.2 L, 13.2 kg, 135.6 mol) was added gradually (approx. 0.5 h) so that the temperature did not exceed 20° C. (jacket temperature at -15° C.). External cooling was discontinued and D-fructose (12.0 kg, 66.6 mol) was added gradually (in 2.0 kg portions) over 2 h while maintaining the temperature between 8°-15° C. The suspension was stirred at room temperature for an additional 2-3 h after all the fructose had dissolved. The solution was then cooled to 5° C. and 50% sodium hydroxide (24.0 kg, 297.6 mol) was added at a rate so as to maintain the solution temperature below 20° C. (addition was complete in 1 h with a jacket temperature at -15° C.). The resulting slurry was centrifuged to remove the precipitated salt (sodium sulfate). Solvent was removed from the filtrate by vacuum distillation and the residual oil was stored at room temperature. The semi-solid reaction product was dissolved in t-butyl methyl ether (48.8 kg, 66.4 L). The solution was washed with distilled water (2×9.0 L) and concentrated to give an oil. The oil was dissolved in hexane (24.0 L)/isopropanol (3.5 L) with gradual warming to 60° C. The product crystallized with cooling. The solid was collected by centrifugation and dried in a vacuum oven at 38° C. for 8.0 h to give 10.8 kg (62.4% yield, 100.8% purity by GLC) of a white solid, mp 95°-96° C.

Workup

  1. customdid not exceed 20° C.
  2. custom(jacket temperature at -15° C.)
  3. temperatureExternal cooling
  4. temperaturewhile maintaining the temperature between 8°-15° C
  5. dissolutionhad dissolved
  6. temperatureto maintain the solution temperature below 20° C. (
  7. additionaddition
  8. customto remove the precipitated salt (sodium sulfate)
  9. customSolvent was removed from the filtrate by vacuum distillation
  10. customwas stored at room temperature
  11. customThe semi-solid reaction product
  12. washThe solution was washed with distilled water (2×9.0 L)
  13. concentrationconcentrated
  14. customto give an oil
  15. temperaturewith gradual warming to 60° C
  16. customThe product crystallized
  17. temperaturewith cooling
  18. customThe solid was collected by centrifugation
  19. customdried in a vacuum oven at 38° C. for 8.0 h
  20. customto give 10.8 kg (62.4% yield, 100.8% purity by GLC) of a white solid, mp 95°-96° C.

Sources & evidence

ORD record
ord-d43663d6b464498cbd06439c3fad2f2d
Source dataset
uspto-grants-1995_02
Patent number
US05387700

Reaction notes

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