Sulfuric Acid → HCID 67099632, compound

HRID 1868743Notes

Reaction equation

HRID 1868743 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:8]([CH3:23])([CH3:22])[C:9]([CH:11]([C:17](OCC)=[O:18])[C:12]([O:14][CH2:15][CH3:16])=[O:13])=[O:10])[CH:5]=[CH:6][CH:7]=1.OS(O)(=O)=O>>[F:1][C:2]1[CH:3]=[C:4]2[C:5]([C:17]([OH:18])=[C:11]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:9](=[O:10])[C:8]2([CH3:22])[CH3:23])=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 1118Sulfuric AcidHCID 67099331HCID 67099331, compound

Product 1

HCID 67099632HCID 67099632, compoundYield 38.3%

Procedure

Diethyl 2-(2-(3-fluorophenyl)-2-methylpropanoyl)malonate (13.03 g, 40 mmol) was added to concentrated H2SO4 (65 mL, 769 mmol), and the mixture was stirred at room temperature for 45 minutes. Ice (H2O) was added, and the aqueous mixture was extracted with EtOAc (2×). The combined organic layers were washed with water (2×) and brine, dried (MgSO4), and concentrated in vacuo to give the crude compound as an orange oil. The crude oil was purified by silica flash chromatography (0-100% DCM/hexane) to give the desired compound as a white solid (4.26 g). MS (m/e)=279.1 (M+H)+.

Workup

  1. additionIce (H2O) was added
  2. extractionthe aqueous mixture was extracted with EtOAc (2×)
  3. washThe combined organic layers were washed with water (2×) and brine
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customto give the crude compound as an orange oil
  7. customThe crude oil was purified by silica flash chromatography (0-100% DCM/hexane)

Sources & evidence

ORD record
ord-06ccc179b47544098590e2aef400812e
Source dataset
uspto-grants-2009_12
Patent number
US07635715B2

Reaction notes

Loading…