Dimethyl Sulfoxide → (3aR,5R,6aS)-5-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyl-3a,6a-dihydrofuro[2,3-d][1,3]dioxol-6-one

HRID 2410434노트

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HRID 2410434 반응식
[C:1](Cl)(=[O:5])[C:2](Cl)=[O:3].[CH3:7]S(C)=O.[CH3:11][C:12]([CH2:14]C(O)(C)C)=O.O[C@H:20]1[O:28][C@H:27]([CH2:29][OH:30])[C@@H:25]([OH:26])[C@H:23]([OH:24])[C@H:21]1O.[Cl-].[NH4+]>ClCCl.O.C(N(CC)CC)C>[CH3:11][C:12]1([CH3:14])[O:5][CH:1]([C@H:23]2[O:24][C@@H:29]3[O:30][C:20]([CH3:21])([CH3:7])[O:28][C@@H:27]3[C:25]2=[O:26])[CH2:2][O:3]1

참가 물질

8

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온도
-75 °C

실험 절차

Oxalyl chloride (25.16 mL) and dichloromethane (200 mL) were taken in a three-neck round bottom flask and cooled to −75° C. under a nitrogen atmosphere. Then dimethylsulfoxide (27.3 mL) was added drop-wise slowly maintaining the temperature at −70° C. The reaction mixture was stirred for 30 minutes at the same temperature, and then diacetone-α-D-glucose (50 g) in dichloromethane (500 mL) was charged slowly, maintaining the temperature at −70° C. After 20 minutes, triethylamine (80 mL) was added drop-wise to the above mixture at the same temperature. A saturated solution of ammonium chloride in water (500 mL) was charged to the reaction mixture after 30 minutes, and the temperature was allowed to rise to room temperature. The reaction mixture was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulphate. The solvent was evaporated under reduced pressure to afford the title compound (45 g).

후처리

  1. temperatureslowly maintaining the temperature at −70° C
  2. temperaturemaintaining the temperature at −70° C
  3. waitAfter 20 minutes
  4. customto rise to room temperature
  5. extractionThe reaction mixture was extracted with dichloromethane
  6. dry with materialThe organic layer was dried over anhydrous sodium sulphate
  7. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-ff8862b6ce5742a594ae9d54b9d9a0ad
출처 데이터셋
uspto-grants-2014_08
특허 번호
US08816073B2

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