반응 #445321

ord-5304b814bb924040bed5fe66f3dbb0bb

반응 방정식

CC(C)=O
acetone
OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
D-mannitol
I
hydriodic acid
CC1(C)OCC(C2OC(C)(C)OC2C2COC(C)(C)O2)O1
1,2:3,4:5,6-tri-O-isopropylidene-D-mannitol
수율 90.0%

시약

없음

용매

반응 조건

온도
60°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the mixture was refluxed
  2. 2
    기타During this reaction
  3. 3
    건조the refluxing solvent was dried with 20 g of Molecular Sieves 3A
  4. 4
    기타After completion of the reaction
  5. 5
    workup.DISTILLATIONThe acetone was then distilled off under reduced pressure
  6. 6
    workup.DISSOLUTIONthe residue was dissolved in chloroform
  7. 7
    세척The solution was washed with aqueous sodium bicarbonate and water
  8. 8
    건조dried over anhydrous magnesium sulfate
  9. 9
    workup.DISTILLATIONThe chloroform was distilled off under reduced pressure

실험 절차

To 200 ml of acetone were added 10.0 g of D-mannitol and 175 mg of hydriodic acid (57%) and the mixture was refluxed with stirring in a water bath at 60° C. for 5 hours. During this reaction, the refluxing solvent was dried with 20 g of Molecular Sieves 3A interposed between the reaction vessel and the cooling jacket. After completion of the reaction, a small amount of pyridine was added. The acetone was then distilled off under reduced pressure and the residue was dissolved in chloroform. The solution was washed with aqueous sodium bicarbonate and water and dried over anhydrous magnesium sulfate. The chloroform was distilled off under reduced pressure to give 15.0 g (90%) of 1,2:3,4:5,6-tri-O-isopropylidene-D-mannitol. After recrystallization from 70% ethanol, it melted at 68.5°-70.5° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04464530uspto-grants-1984_08