Sulfuric Acid → HCID 67099311, compound

HRID 1868728Notes

Reaction equation

HRID 1868728 reaction equation
OS(O)(=O)=O.O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[Cl:20][C:21]1[CH:22]=[C:23]([C:27]([CH3:43])([CH2:41][CH3:42])[C:28]([CH:30]([C:36]([O:38][CH2:39][CH3:40])=[O:37])[C:31](OCC)=[O:32])=[O:29])[CH:24]=[CH:25][CH:26]=1>>[Cl:20][C:21]1[CH:22]=[C:23]2[C:24]([C:31]([OH:32])=[C:30]([C:36]([O:38][CH2:39][CH3:40])=[O:37])[C:28](=[O:29])[C:27]2([CH2:41][CH3:42])[CH3:43])=[CH:25][CH:26]=1

Participants

4

Procedure

H2SO4 (40 mL, 473 mmol) was cooled to 0° C. and treated with P2O5 (15 g, 106 mmol). The mixture was brought to room temperature and added to diethyl 2-(2-(3-chlorophenyl)-2-methylbutanoyl)malonate (7.67 g, 22 mmol). The reaction mixture was then stirred for 1.5 hours. Ice (H2O) was added, and the aqueous mixture was extracted with EtOAc (3×). 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 yellow solid (3.16 g). MS (m/e)=309.1 (M+H)+.

Workup

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

Sources & evidence

ORD record
ord-40644f50f79a44aeaec677615a816e4e
Source dataset
uspto-grants-2009_12
Patent number
US07635715B2

Reaction notes

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