Potassium Carbonate → HCID 86603897, compound

HRID 1171181Notes

Reaction equation

HRID 1171181 reaction equation
[CH2:1]([O:3][C:4](=[O:14])[CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([OH:13])[CH:8]=1)[CH3:2].C([O-])([O-])=O.[K+].[K+].[CH2:21]1[O:23][C@H:22]1[CH2:24]OS(C1C=C([N+]([O-])=O)C=CC=1)(=O)=O>CC(C)=O>[CH2:1]([O:3][C:4](=[O:14])[CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH2:24][C@H:22]2[CH2:21][O:23]2)[CH:8]=1)[CH3:2]

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 146513Benzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl esterHCID 15197885Ethyl 3-(3-hydroxyphenyl)propanoate

Product 1

HCID 86603897HCID 86603897, compoundYield 93%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

To an acetone solution (0.15 M, 170 mL) of 3-(3-Hydroxy-phenyl)-propionic acid ethyl ester (5.0 g, 25.77 mmol) was added K2CO3 (10.69 g, 77.32 mmol), and the mixture was heated to reflux for 30 min. After cooling this mixture to RT, (2R)-(−)-glycidyl 3-nitrobenzenesulfonate (6.68 g, 25.77 mmol) was added, and the resulting mixture was heated to reflux overnight. After cooling to room temperature, the solids were removed by filtration and washed well with ethyl acetate. The filtrate was concentrated and partitioned between ethyl acetate and 1N HCl. The organic portion was washed successively with 5% NaHCO3 and brine, dried (MgSO4), filtered and concentrated to a solid. Purification by FCC (30% ethyl acetate/hexanes) gave the product as a white solid in 93% yield (6.0 g). LCMS (m/z) M+H: 187

Workup

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 30 min
  3. temperaturethe resulting mixture was heated
  4. temperatureto reflux overnight
  5. temperatureAfter cooling to room temperature
  6. customthe solids were removed by filtration
  7. washwashed well with ethyl acetate
  8. concentrationThe filtrate was concentrated
  9. custompartitioned between ethyl acetate and 1N HCl
  10. washThe organic portion was washed successively with 5% NaHCO3 and brine
  11. dry with materialdried (MgSO4)
  12. filtrationfiltered
  13. concentrationconcentrated to a solid
  14. customPurification by FCC (30% ethyl acetate/hexanes)

Sources & evidence

ORD record
ord-4b329c1dd256448b8a748428eeb91ab9
Source dataset
uspto-grants-2010_11
Patent number
US07829594B2

Reaction notes

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