Acetone → HCID 57772123, compound

HRID 2405173Notes

Reaction equation

HRID 2405173 reaction equation
[CH:1]1[C:5]2=[C:6](O)[C:7]3[CH:14]=[CH:13][C:11](=[O:12])[O:10][C:8]=3[CH:9]=[C:4]2[O:3][CH:2]=1.[C:16]([O-])([O-])=[O:17].[K+].[K+].[I-].[Na+].P(O)([O-])([O-])=[O:25].[Na+].[Na+].[CH3:31][C:32]([CH3:34])=[O:33]>>[CH3:16][O:17][C:31](=[O:25])[CH:32]([O:33][C:6]1[C:5]2[CH:1]=[CH:2][O:3][C:4]=2[CH:9]=[C:8]2[C:7]=1[CH:14]=[CH:13][C:11](=[O:12])[O:10]2)[CH3:34]

Participants

6

Procedure

To a mixture of Bergaptol (10 grams, 49.5 mmol), anhydrous K2CO3 (20 grams, 144.7 mmol), Sodium iodide (2.4 grams, 16 mmol), disodium phosphate (2.4 grams, 17 mmol) in anhydrous acetone (250 mL) was added methyl 2-chloro propionate (10 mL, 87.7 mmol) and refluxed for 8 hours. Acetone was distilled and water (100 mL) was added. Crude 40 was filtered and recrystallized in a mixture of methanol:chloroform (9:1) to give pure 40 (5.5 grams, 38.5%) as a white powder. The melting point was found to be 149.6-151.6° C. The structure was confirmed with IR and NMR. IHNMR (CDCl3) δ 1.78(d, 3H,—CH3), 3.68(s, 3H, ester), 5.18(q, 1H, CH), 6.31(d, 1H, J=12.1 Hz, pyran), 6.84(d, 1H, J=1.1 Hz, furan), 7.22(s, 1H, Ar), 7.64(d, 1H, J=1.1 Hz, furan), 8.36(d, 1H, J=12.1 Hz, pyran).

Workup

  1. temperaturerefluxed for 8 hours
  2. distillationAcetone was distilled
  3. additionwater (100 mL) was added
  4. filtrationCrude 40 was filtered
  5. customrecrystallized in a mixture of methanol:chloroform (9:1)

Sources & evidence

ORD record
ord-a7623e2a76eb4d59baf94a3b8571dc1f
Source dataset
uspto-grants-2014_08
Patent number
US08802892B2

Reaction notes

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