HCID 13565763, compound → HCID 13984538, compound
Reaction equation
[OH:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][C:12]=3[OH:17])[CH:7]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[C:6]=2[CH:5]=[CH:4][CH:3]=1>C(OC(=O)CC)(=O)CC.N1C=CC=CC=1>[C:18]1([C:7]2[C:6]3[C:15](=[C:2]([O:1][C:12](=[O:17])[CH2:11][CH3:10])[CH:3]=[CH:4][CH:5]=3)[C:14]([O:16][C:14](=[O:16])[CH2:13][CH3:8])=[C:13]3[C:8]=2[CH:9]=[CH:10][CH:11]=[C:12]3[O:17][C:2](=[O:1])[CH2:3][CH3:4])[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a mixture, stirred under an argon atmosphere, of 2.5 g of 1,8-dihydroxy-10-phenyl anthrone obtained at example 10 (1) in 25 cm3 of propionic anhydride, 0.100 cm3 of anhydrous pyridine is added. The reaction mixture is then brought for one hour to 70° C., at the end of which period all the initial reactant is transformed. The reactive excess is then removed by evaporation under a vacuum. The resulting solid is dissolved in a minimum of toluene, introduced into a silica gel column and then eluted with toluene. After evaporation of the eluant, 1.3 g of a solid are obtained which is then recrystallized in a toluene/hexane mixture, yielding 1.1 g white crystals having a melting point of 216° C.
Workup
- additionis added
- customThe reactive excess is then removed by evaporation under a vacuum
- dissolutionThe resulting solid is dissolved in a minimum of toluene
- additionintroduced into a silica gel column
- washeluted with toluene
- customAfter evaporation of the eluant, 1.3 g of a solid
- customare obtained which
- customis then recrystallized in a toluene/hexane mixture
Sources & evidence
- ORD record
- ord-774ffb11453d47a8908e3c8531b4c871
- Source dataset
- uspto-grants-1989_06
- Patent number
- US04843097
Reaction notes
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