Potassium Carbonate → HCID 69411429, compound

HRID 1350338Notes

Reaction equation

HRID 1350338 reaction equation
[CH2:1]([O:8][C:9]([C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([C:18]([O:20][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)=[O:19])[CH:12]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:34][O:35][C:36](=[O:39])[CH2:37]Br>CN(C=O)C.C(OCC)(=O)C>[CH2:1]([O:8][C:9](=[O:10])[C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:37][C:36]([O:35][CH3:34])=[O:39])=[C:13]([C:18]([O:20][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)=[O:19])[CH:12]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

6

Conditions

Temperature
50 °C

Procedure

In DMF (15 mL) was stirred 4-hydroxy-1,3-benzenedicarboxylate dibenzyl ester (500 mg, 1.4 mmol) and potassium carbonate (276 mg, 2.0 mmol). To this was added methylbromoacetate (230 mg, 1.5 mmol) and the solution warmed to 50° C. and stirred 120 hours. The mixture filtered free of insoluble material and the DMF solution evaporated at reduced pressure to give a red oil. The oil was dissolved in ethyl acetate (50 mL) and washed successively with 10% citric acid (50 ML), saturated sodium bicarbonate solution (50 mL), and brine (50 mL). The organic phase dried over magnesium sulfate and evaporated at reduced pressure to give an oil. The oil was purified by MPLC (90 g silica gel, 2:1[hexane:ethyl acetate]) to give 330 mg (54%) of a clear oil. MS: M+1=435.2.

Workup

  1. filtrationThe mixture filtered free of insoluble material
  2. customthe DMF solution evaporated at reduced pressure
  3. customto give a red oil
  4. washwashed successively with 10% citric acid (50 ML), saturated sodium bicarbonate solution (50 mL), and brine (50 mL)
  5. dry with materialThe organic phase dried over magnesium sulfate
  6. customevaporated at reduced pressure
  7. customto give an oil
  8. customThe oil was purified by MPLC (90 g silica gel, 2:1[hexane:ethyl acetate])

Sources & evidence

ORD record
ord-44452b16c2cf41da818d1bb54f006fe3
Source dataset
uspto-grants-2007_05
Patent number
US07214712B2

Reaction notes

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