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Toluene → 2,3,4,6-Tetra-O-acetyl-beta-D-glucopyranosyl chloride

HRID 842303
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HRID 842303 반응식
C(O[C@@H:5]1[O:22][C@H:21]([CH2:23][O:24][C:25](=[O:27])[CH3:26])[C@@H:16]([O:17][C:18](=[O:20])[CH3:19])[C@H:11]([O:12][C:13](=[O:15])[CH3:14])[C@H:6]1[O:7][C:8](=[O:10])[CH3:9])(=O)C.[Al+3].[Cl-:29].[Cl-].[Cl-].C1(C)C=CC=CC=1.[Si](O)(O)(O)O>C(Cl)(Cl)Cl>[CH3:26][C:25]([O:24][CH2:23][C@H:21]1[O:22][C@@H:5]([Cl:29])[C@H:6]([O:7][C:8]([CH3:9])=[O:10])[C@@H:11]([O:12][C:13]([CH3:14])=[O:15])[C@@H:16]1[O:17][C:18]([CH3:19])=[O:20])=[O:27]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1140TolueneHCID 14942Orthosilicic acidHCID 2724702beta-D-Glucose pentaacetateHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 109595272,3,4,6-Tetra-O-acetyl-beta-D-glucopyranosyl chloride

시약·촉매·용매 1

HCID 6212Chloroform
용매

실험 절차

To a solution of β-D-glucose pentaacetate (20 g) in CHCl3 (100 mL) was added AlCl3 (3.6 g). After stirring at room temperature, toluene (100 mL) was added, followed by silicic acid (2 g). The mixture was stirred for a few minutes and the precipitate was removed by filtration. The solution was partially concentrated under vacuum and extracted with ice cold water (25 mL). The organic phase was concentrated to a syrupy mixture and ether was added to precipitate acetochloro-β-D-glucose as a powder (12 g).

후처리

  1. stirringThe mixture was stirred for a few minutes
  2. customthe precipitate was removed by filtration
  3. concentrationThe solution was partially concentrated under vacuum
  4. extractionextracted with ice cold water (25 mL)
  5. concentrationThe organic phase was concentrated to a syrupy mixture and ether
  6. additionwas added
  7. customto precipitate acetochloro-β-D-glucose as a powder (12 g)

출처 및 근거

ORD 기록
ord-1852d66a299b432399841ac1a344b597
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06372895B1

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