Sulfuric Acid → HCID 67099792, compound

HRID 2078115Notes

Reaction equation

HRID 2078115 reaction equation
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.OS(O)(=O)=O.[Cl:20][C:21]1[C:26]([Cl:27])=[CH:25][CH:24]=[CH:23][C:22]=1[C:28]([CH3:43])([CH3:42])[C:29]([CH:31]([C:37]([O:39][CH2:40][CH3:41])=[O:38])[C:32]([O:34]CC)=O)=[O:30]>>[Cl:27][C:26]1[C:21]([Cl:20])=[C:22]2[C:23]([C:32]([OH:34])=[C:31]([C:37]([O:39][CH2:40][CH3:41])=[O:38])[C:29](=[O:30])[C:28]2([CH3:42])[CH3:43])=[CH:24][CH:25]=1

Participants

4

Conditions

Temperature
25 °C

Procedure

P2O5 (5.00 g, 35 mmol) was treated with H2SO4 (4.5 mL, 81 mmol) at 0° C. in a 100 mL round bottom flask. Diethyl 2-(2-(2,3-dichlorophenyl)-2-methylpropanoyl)malonate (0.500 g, 1.0 mmol) was added, and the mixture was stirred at 25° C. for 1.5 hours. The reaction was quenched with ice, extracted with EtOAc (2×50 mL), and the combined organic layers were washed with brine (50 mL). The organic layers were then dried over MgSO4, concentrated, and dried in vacuo to give the title compound (0.235 g). MS m/e=329 (M+H)+.

Workup

  1. customThe reaction was quenched with ice
  2. extractionextracted with EtOAc (2×50 mL)
  3. washthe combined organic layers were washed with brine (50 mL)
  4. dry with materialThe organic layers were then dried over MgSO4
  5. concentrationconcentrated
  6. customdried in vacuo

Sources & evidence

ORD record
ord-3e4e761602f74eeca1e206788a7ad404
Source dataset
uspto-grants-2011_04
Patent number
US07928139B2

Reaction notes

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