Benzoic Acid → HCID 20437622, compound
Reaction equation
[O-2:1].[Mg+2:2].[Cl:3][C:4]1[CH:13]=[CH:12][C:7]([C:8]([O:10][OH:11])=[O:9])=[CH:6][CH:5]=1.[C:14]([OH:22])(=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C(OCC)(=O)C.O>[OH2:9].[OH2:21].[OH2:1].[OH2:9].[Cl:3][C:4]1[CH:13]=[CH:12][C:7]([C:8]([O:10][O-:11])=[O:9])=[CH:6][CH:5]=1.[C:14]([O-:22])(=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[Mg+2:2]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Magnesium oxide (0.443 g, 11.0 mmol) was added to a solution of 4-chloroperoxybenzoic acid (94.6%, 2.00 g, 11.0 mmol) and benzoic acid (1.26 g, 10.3 mmol) in 65 mL of ethyl acetate and 0.80 mL of water. After 90 min of vigorous stirring, the precipitate was collected via filtration, washed with ethyl acetate (ca. 50 mL), and vacuum dried to give 3.50 g (82% based on Mg2+) of a white powder: Anal. Calcd for C14H17ClMgO9 : C, 43.22; H, 4.40; Cl, 9.11; Mg, 6.25; O(active), 4.11. Found: C, 43.88; H, 4.07; Cl, 9.79; Mg, 6.80; O(active), 3.95.
Workup
- filtrationthe precipitate was collected via filtration
- washwashed with ethyl acetate (ca. 50 mL), and vacuum
- customdried
- customto give 3.50 g (82% based on Mg2+) of a white powder
Sources & evidence
- ORD record
- ord-cbeeb1d9264b4623ae3bab39c4867db8
- Source dataset
- uspto-grants-1984_11
- Patent number
- US04483781
Reaction notes
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