Lithium Hydroxide → HCID 10692663, compound

HRID 1464814Notes

Reaction equation

HRID 1464814 reaction equation
[CH2:1]([O:3][C@H:4]([C:28](N1[C@@H](CC2C=CC=CC=2)COC1=O)=[O:29])[CH2:5][C:6]1[CH:7]=[CH:8][C:9]2[O:13][C:12]([CH2:14][C:15]3[N:16]=[C:17]([C:21]4[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=4)[O:18][C:19]=3[CH3:20])=[CH:11][C:10]=2[CH:27]=1)[CH3:2].[OH-:43].[Li+]>O1CCCC1>[CH2:1]([O:3][C@@H:4]([CH2:5][C:6]1[CH:7]=[CH:8][C:9]2[O:13][C:12]([CH2:14][C:15]3[N:16]=[C:17]([C:21]4[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=4)[O:18][C:19]=3[CH3:20])=[CH:11][C:10]=2[CH:27]=1)[C:28]([OH:29])=[O:43])[CH3:2]

Participants

4

Reactant 2

HCID 3939Lithium HydroxideHCID 10530982HCID 10530982, compound

Product 1

HCID 10692663HCID 10692663, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
0 °C

Procedure

5-((S)-2-Ethoxy-3[(S)-4-benzyl-2-oxo-3-oxazolidinyl]-3-oxopropyl}-2-[(5-methyl-2-phenyl-4-oxazolyl)methyl]benzofuran (0.15 g, 0.26 mmol) was dissolved in tetrahydrofuran (5 ml). The solution was cooled to 0° C. and 0.5N lithium hydroxide (1.1 ml, 0.52 mmol) was added. After 15 minutes the bulk of the ethanol was removed, the residue was acidified with 1N HCl, diluted with water and extracted with ethyl acetate (3×). The combined extracts were washed with brine, dried over sodium sulfate and concentrated. The product was purified by flash chromatography (hexanes/ethyl acetate/acetic acid, 10:10:1) then recrystallized from hexanes/ethyl acetate and obtained as a white solid (48 mg, m.p. 129° C., [α]D =-12.5° (c 0.99, CDCl3)):

Workup

  1. customAfter 15 minutes the bulk of the ethanol was removed
  2. additiondiluted with water
  3. extractionextracted with ethyl acetate (3×)
  4. washThe combined extracts were washed with brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated
  7. customThe product was purified by flash chromatography (hexanes/ethyl acetate/acetic acid, 10:10:1)
  8. customthen recrystallized from hexanes/ethyl acetate
  9. customobtained as a white solid (48 mg, m.p. 129° C., [α]D =-12.5° (c 0.99, CDCl3))

Sources & evidence

ORD record
ord-ccbeb8ae894145bb9f08f6c02c092fa0
Source dataset
uspto-grants-1994_04
Patent number
US05306726

Reaction notes

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