D-glucaro-1,4:6,3-dilactone → (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

HRID 1004482

반응식

HRID 1004482 반응식
[C:1]1(=[O:12])[O:11][C@@H:5]2[C@@H:6]([C:8]([O:10][C@@H:4]2[C@H:2]1[OH:3])=[O:9])[OH:7]>O>[O:9]=[CH:8][C@@H:6]([C@H:5]([C@@H:4]([C@@H:2]([CH2:1][OH:12])[OH:3])[OH:10])[OH:11])[OH:7]

참가 물질

3

실험 절차

Isolation of crystalline D-glucaro-1,4:6,3-dilactone--The syrup was transferred with a few mL of water to a large 1 L round-bottom flask and then concentrated under reduced pressure to a tacky solid. The flask was placed in a vacuum desiccator set at <0.1 torr and 50° C. for 5 hours. As a result of this treatment, the solid swelled into a white foam filling the flask. The flask was removed from the desiccator and the foam was broken up within the flask and stirred to a powder using a spatula. The powder in the flask was returned to the vacuum desiccator where it remained for 36 hours at <0.1 torr and approximately 45° C. A sample of the resultant beige colored powder was subjected to 1H NMR analysis. The analysis indicated that virtually all of the glucaric acid present had been converted to D-glucaro-1,4:6,3-dilactone. 40 mL of dioxane was added to the flask and the powder dissolved with vigorous shaking. When this solution was transferred to a smaller 250 mL round-bottom flask, D-glucaro-1,4:6,3-dilactone crystals (which is a direct crystalline form of glucaric acid) began to form spontaneously. The 250 mL flask was placed in a desiccator and crystallization was allowed to continue overnight. The crystal mass was stirred to a slurry, and the mother liquor was removed by suction in a Buchner funnel. The crystals were washed once with approximately 15 mL of a cold 3:1 (v/v) mixture of dioxane:CH2Cl2 and placed in a desiccator for 24 hours at 45° C. The weight of the crystals was 5.83 g which is 24.1% of the theoretical yield from glucose.

후처리

  1. concentrationconcentrated under reduced pressure to a tacky solid
  2. customAs a result of this treatment
  3. customThe flask was removed from the desiccator
  4. waitremained for 36 hours at <0.1 torr and approximately 45° C
  5. addition40 mL of dioxane was added to the flask
  6. dissolutionthe powder dissolved with vigorous shaking
  7. customWhen this solution was transferred to a smaller 250 mL round-bottom flask
  8. customto form spontaneously
  9. customThe 250 mL flask was placed in a desiccator
  10. customcrystallization
  11. waitto continue overnight
  12. stirringThe crystal mass was stirred to a slurry
  13. customthe mother liquor was removed by suction in a Buchner funnel
  14. washThe crystals were washed once with approximately 15 mL of a cold 3:1 (v/v) mixture of dioxane
  15. waitCH2Cl2 and placed in a desiccator for 24 hours at 45° C

출처 및 근거

ORD 기록
ord-b93f1aaa99a84a51aa001ea72d8ef1f8
출처 데이터셋
uspto-grants-2000_04
특허 번호
US06049004

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