Sulfuric Acid → HCID 67099551, compound
Reaction equation
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.OS(O)(=O)=O.[F:20][C:21]1[CH:22]=[C:23]([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])[CH:24]=[CH:25][C:26]=1[F:27]>CCOC(C)=O>[CH2:40]([O:39][C:37]([C:31]1[C:29](=[O:30])[C:28]([CH3:43])([CH3:42])[C:23]2[C:24]([C:32]=1[OH:34])=[CH:25][C:26]([F:27])=[C:21]([F:20])[CH:22]=2)=[O:38])[CH3:41]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
P2O5 (26.9 g, 189 mmol) was added to concentrated H2SO4 (50.5 mL) at 0° C. Diethyl 2-(2-(3,4-difluorophenyl)-2-methylpropanoyl)malonate (32.42 g, 94.7 mmol) was added at 0° C., and the reaction mixture was allowed to warm to ambient temperature and stirred for 16 hours. The resulting reaction mixture was then poured into ice, diluted with 400 mL of EtOAc, added to a separatory funnel, partitioned with water, washed 3 times with 75 mL of water, separated, dried over Na2SO4, and concentrated in vacuo to give the title compound as a beige yellow amorphous solid which was used without further purification. MS (m/z)=297 (M+H)+.
Workup
- customThe resulting reaction mixture
- additionwas then poured into ice
- additionadded to a separatory funnel
- custompartitioned with water
- washwashed 3 times with 75 mL of water
- customseparated
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-4788874853cc41588bdbbef3c371a6dd
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07635715B2
Reaction notes
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