4-Chlororesorcinol → HCID 67166662, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[OH:9].[Cl:10][CH2:11][CH2:12][C:13](O)=[O:14].C(OCC)(=O)C>FC(F)(F)S(O)(=O)=O>[Cl:10][CH2:11][CH2:12][C:13]([C:6]1[CH:7]=[C:2]([Cl:1])[C:3]([OH:9])=[CH:4][C:5]=1[OH:8])=[O:14]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 4-chlorobenzene-1,3-diol (100 g, 692 mmol) and 3-chloropropanoic acid (75.1 g, 692 mmol) in trifluoromethanesulfonic acid (295 ml) was stirred at 75° C. for 30 minutes. The reaction was cooled to ambient temperature and slowly poured into a 2 L beaker filled with ice. To the slurry was added ethyl acetate with stirring until all solids dissolved. The mixture was poured into a separatory funnel, the aqueous layer was removed and the resulting organic layer was washed with water. The organic layer was dried over magnesium sulfate, filtered and concentrated. The residue was purified by column chromatograph (silica) eluting with a solvent system mixture of 15% ethyl acetate/hexanes to provide the desired product (162.6 g, 86%).
Workup
- additionslowly poured into a 2 L
- additionbeaker filled with ice
- dissolutiondissolved
- additionThe mixture was poured into a separatory funnel
- customthe aqueous layer was removed
- washthe resulting organic layer was washed with water
- dry with materialThe organic layer was dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified by column chromatograph (silica)
- washeluting with a solvent system mixture of 15% ethyl acetate/hexanes
Sources & evidence
- ORD record
- ord-71f8d4801ae148508d85a78eeb666a9c
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08785445B2
Reaction notes
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