Sodium Carbonate → HCID 67697613, compound

HRID 1938775Notes

Reaction equation

HRID 1938775 reaction equation
[C:1]([C@H:6]1[O:10][C@H:9](C(=O)C)[CH2:8][O:7]1)([O:3][CH2:4][CH3:5])=[O:2].C1C=C(Cl)C=[C:16]([C:21]([O:23]O)=[O:22])C=1.C(=O)([O-])[O-].[Na+].[Na+]>ClCCl.O>[C:1]([C@H:6]1[O:10][C@H:9]([O:23][C:21](=[O:22])[CH3:16])[CH2:8][O:7]1)([O:3][CH2:4][CH3:5])=[O:2]

Participants

6

Procedure

A 2.5:1 mixture of cis and trans-2-carboethoxy-4-acetyl-1,3-dioxolane (406 mg, 2.16 mmol), 85% mCPBA (68 mg, 3.81 mmol) and sodium carbonate (389 mg, 3.67 mmol) in dry dichloromethane (10 mL) was stirred under argon for 16 hours at room temperature. The resultant suspension was diluted with dichloromethane and water and stirred for 10 minutes. The aqueous phase was removed and the organic phase was washed successively with saturated sodium thiosulfate, water, brine and then was dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the crude product thus obtained was subjected to flash column chromatography (30% EtOAc-Hexanes) to give the title compound (49% yield) which displayed the following spectral characteristics; 1H NMR (CDCl3): δ 1.29 (t, 3H, J=7.2 Hz), 2.09 (s, 1H), 4.12 (d of d, 1H, J=0.9, 9.1 Hz), 4.19-4.31 (m, 3H), 5.53 (s, 1H), 6.48 (d of d, 1H, J=0.9, 3.9 Hz).

Workup

  1. stirringstirred for 10 minutes
  2. customThe aqueous phase was removed
  3. washthe organic phase was washed successively with saturated sodium thiosulfate, water, brine
  4. dry with materialwas dried over anhydrous magnesium sulfate
  5. customThe solvent was removed under reduced pressure
  6. customthe crude product thus obtained

Sources & evidence

ORD record
ord-b7c220427da34273a92371ab5c9dc7eb
Source dataset
uspto-grants-1997_12
Patent number
US05693787

Reaction notes

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