Potassium sodium tartarate → HCID 10705537, compound

HRID 2086205Notes

Reaction equation

HRID 2086205 reaction equation
[C:1]([O:5][C:6]([N:8]1[C@:12]([CH2:14][O:15]C(=O)CCCCC)([CH3:13])[CH2:11][O:10][C:9]1([CH3:24])[CH3:23])=[O:7])([CH3:4])([CH3:3])[CH3:2].[H-].C([Al+]CC(C)C)C(C)C.C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>ClCCl>[C:1]([O:5][C:6]([N:8]1[C@:12]([CH2:14][OH:15])([CH3:13])[CH2:11][O:10][C:9]1([CH3:24])[CH3:23])=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

5

Conditions

Temperature
-78 °C

Procedure

3-t-Butoxycarbonyl-2,2-dimethyl-(4R)-n-hexanoyloxymethyl-4-methyloxazolidine (13.7 g, 39.9 mmol) obtained in Reference example 2(a) was dissolved in dichloromethane (200 ml), and the hexane solution of 1.0M diisobutylaluminium hydride (99 ml, 99.7 mmol) was added dropwise thereto at −78° C. After, the reaction mixture was stirred for 30 minutes at −78° C., cooled down to room temperature, and 10 wt % aqueous potassium sodium tartrate solution (200 ml) was added thereto followed by stirring vigorously for 30 minutes. The reaction solution was extracted with diethyl ether, and after the ether layer was dried over anhydrous sodium sulfate, the solvent was evaporated in vacuo. The residue was purified by flash chromatography on a silica gel column (elution solvent; n-hexane:ethyl acetate=5:2) to afford the title compound (10.5 g, 100% yield) as a white crystalline solid.

Workup

  1. customat −78° C
  2. temperaturecooled down to room temperature
  3. stirringby stirring vigorously for 30 minutes
  4. extractionThe reaction solution was extracted with diethyl ether
  5. dry with materialafter the ether layer was dried over anhydrous sodium sulfate
  6. customthe solvent was evaporated in vacuo
  7. customThe residue was purified by flash chromatography on a silica gel column (elution solvent; n-hexane:ethyl acetate=5:2)

Sources & evidence

ORD record
ord-e71cff69672a4f68be7dda4585d36096
Source dataset
uspto-grants-2004_04
Patent number
US06723745B2

Reaction notes

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