Sulfuric Acid → HCID 67099311, compound
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]=1Participants
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
- customwas brought to room temperature
- additionIce (H2O) was added
- extractionthe aqueous mixture was extracted with EtOAc (3×)
- washThe combined organic layers were washed with water (2×) and brine
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customto give the crude compound as an orange oil
- customThe crude oil was purified by silica flash chromatography (0-100% DCM/hexane)
Sources & evidence
- ORD record
- ord-ea7fe8ad95194750b3eea67a871bef84
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07928139B2
Reaction notes
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