Ethylene Glycol → 2-Pyridinyl-1,3-dioxolane

HRID 742456

반응식

HRID 742456 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH:7]=[O:8].[CH2:9](O)[CH2:10][OH:11].O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[O:8]1[CH2:9][CH2:10][O:11][CH:7]1[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=1

참가 물질

5

반응물 3

HCID 174Ethylene GlycolHCID 142732-PyridinecarboxaldehydeHCID 521998p-Toluenesulfonic acid monohydrate

생성물 1

HCID 797732-Pyridinyl-1,3-dioxolane

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of pyridine-2-carboxaldehyde (151 g, 1.41 mol), ethylene glycol (157 mL), and 56 g (0.29 mol) of p-toluenesulfonic acid monohydrate in 1.4 L of toluene placed in a 5 L flask fitted with a Dean Stark trap was heated to reflux for 16 h, removing 50 mL of water. The mixture was concentrated in vacuo to a 800 mL volume, cooled, saturated sodium hydrogen carbonate solution was added (to pH 8-9), the layers were separated and the aqueous layer was washed with 100 mL of toluene. The combined organic layer was dried over magnesium sulfate, concentrated in vacuo, and distilled (with a short distilling head) to afford 119.5 g of 2-(1,3-dioxolan-2-yl)-pyridine (Formula V: R1 =H) as a pale oil, b.p. 100° C./1 mm.

후처리

  1. customplaced in a 5 L flask
  2. customfitted with a Dean Stark trap
  3. temperaturewas heated
  4. temperatureto reflux for 16 h
  5. customremoving 50 mL of water
  6. concentrationThe mixture was concentrated in vacuo to a 800 mL volume
  7. temperaturecooled
  8. additionsaturated sodium hydrogen carbonate solution was added (to pH 8-9)
  9. customthe layers were separated
  10. washthe aqueous layer was washed with 100 mL of toluene
  11. dry with materialThe combined organic layer was dried over magnesium sulfate
  12. concentrationconcentrated in vacuo
  13. distillationdistilled (with a short distilling head)

출처 및 근거

ORD 기록
ord-088d172f8141412da8a60f0a7d102694
출처 데이터셋
uspto-grants-1996_09
특허 번호
US05554620

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