Dihydroxyacetone → 2-Propanone, 1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]-

HRID 1679031Notes

Reaction equation

HRID 1679031 reaction equation
[O:1]1[CH:6]=[CH:5][CH2:4][CH2:3][CH2:2]1.[OH:7][CH2:8][C:9](=[O:12])[CH2:10][OH:11]>Cl>[O:1]1[CH2:2][CH2:3][CH2:4][CH2:5][CH:6]1[O:7][CH2:8][C:9](=[O:12])[CH2:10][O:11][CH:2]1[CH2:3][CH2:4][CH2:5][CH2:6][O:1]1

Participants

4

Conditions

Temperature
85 °C

Procedure

A mixture of 236.3 g 3,4-dihydropyran and 90.1 g 1,3-dihydroxy-2-propanone, to which had been added 20 drops of concentrated hydrochloric acid, was heated to 85° C at which temperature, an exothermic reaction began. A cooling bath was applied to maintain the temperature in the range 85°-95° C during the next 15 minutes when heat was again applied to maintain the temperature at 85°-95° C for 2 hours. Excess dihydropyran was removed by warming under reduced pressure and the residue was dissolved in 600 ml of diethyl ether. The ether solution was washed (4 × 200 ml) with 5% aqueous sodium carbonate, then with water (3 × 300 ml) and dried over magnesium sulfate. The dried solution was distilled under reduced pressure to give 172.7 g of 1,3-bis(2-tetrahydropyranyloxy)-2-propanone, b.p. 90°-97°/2 × 10-4 mm.

Workup

  1. customan exothermic reaction
  2. customA cooling bath was applied
  3. temperatureto maintain the temperature in the range 85°-95° C during the next 15 minutes when
  4. temperatureheat
  5. temperatureto maintain the temperature at 85°-95° C for 2 hours
  6. customExcess dihydropyran was removed
  7. temperatureby warming under reduced pressure
  8. dissolutionthe residue was dissolved in 600 ml of diethyl ether
  9. washThe ether solution was washed (4 × 200 ml) with 5% aqueous sodium carbonate
  10. dry with materialwith water (3 × 300 ml) and dried over magnesium sulfate
  11. distillationThe dried solution was distilled under reduced pressure

Sources & evidence

ORD record
ord-9780089556d1415faf5812c03d4f4035
Source dataset
uspto-grants-1978_03
Patent number
US04077982

Reaction notes

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