Methanol → (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

HRID 1841670Notes

Reaction equation

HRID 1841670 reaction equation
C([C@:4]1([OH:19])[C@H:9]([OH:10])[C@@H:8]([CH2:11][OH:12])[O:7]C(C(=O)C)=[C:5]1[C:16](=[O:18])C)(=O)C.[Li+].[Br-].CO.O.C1(C)C=CC(S(O)(=O)=[O:32])=CC=1>CC#N>[O:12]=[CH:11][C@@H:8]([C@H:9]([C@@H:4]([C@@H:5]([CH2:16][OH:18])[OH:32])[OH:19])[OH:10])[OH:7]

Participants

6

Reactant 4

HCID 887MethanolHCID 82050Lithium BromideHCID 521998p-Toluenesulfonic acid monohydrateHCID 22843480HCID 22843480, compound

Product 1

HCID 107526(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

To a solution of the crude triacetyl glucal 3 (9.54 g, 35.0 mmol) in CH3CN (150 mL) was successively added LiBr (3.65 g, 42.0 mmol), MeOH (2.25 g, 70.2 mmol), and p-toluenesulfonic acid monohydrate (p-TsOH.H20, 954 mg) at room temperature. After being stirred for 3 h, the reaction mixture was concentrated to a small volume, diluted with cold 5% NaHCO3 solution, and extracted with CHCl3. The organic extract was washed with ice-water, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed on silica gel (150 g) using 30% AcOEt-hexane to give 8 (9.01 g, 92% from D-glucose) (α-anomer:β-anomer=ca. 10:1). 8a was isolated as a single isomer, while 8b was obtained as a mixture of 8a and 8b.

Workup

  1. customat room temperature
  2. concentrationthe reaction mixture was concentrated to a small volume
  3. additiondiluted with cold 5% NaHCO3 solution
  4. extractionextracted with CHCl3
  5. extractionThe organic extract
  6. washwas washed with ice-water
  7. dry with materialdried over MgSO4
  8. customevaporated in vacuo
  9. customThe residue was chromatographed on silica gel (150 g)

Sources & evidence

ORD record
ord-6e0df9b4e86b4a938f509035245d7502
Source dataset
uspto-grants-2004_01
Patent number
US06683219B2

Reaction notes

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