Acetoacetic Acid → HCID 69868084, compound
Reaction equation
[CH2:1]([C@:3]12[CH2:11][CH2:10][C@@H:9]3[C@@H:12]4[C:17](=[CH:18][CH2:19][C@H:8]3[C@@H:7]1[CH2:6][CH2:5][CH:4]2[OH:21])[CH:16]=[C:15]([OH:20])[CH2:14][CH2:13]4)[CH3:2].[CH3:22][C:23](CC(O)=O)=[O:24].BrN1C(=O)CCC1=O>CC(C)=O.N1C=CC=CC=1.C([O-])(=O)C.[Na+].O.C(O)(=O)C>[CH2:1]([C@:3]12[CH2:11][CH2:10][C@@H:9]3[C@@H:12]4[C:17]([CH:18]=[CH:19][C@H:8]3[C@@H:7]1[CH2:6][CH2:5][C@@H:4]2[O:21][C:23](=[O:24])[CH3:22])=[CH:16][C:15](=[O:20])[CH2:14][CH2:13]4)[CH3:2]Participants
Procedure
Add dl-13-ethyl-3,17-dihydroxygona-3,5-diene, diacetate (1.0 g) dissolved in acetone (20 cc) to a solution of acetone (86 cc), pyridine (.59 ml), sodium acetate (2.72 cc), water (27.2 cc) and acetic acid (2.72 cc). Chill to 0° and add N-bromosuccinimide (0.5 g). Stir for three hours at a temperature between +5° and -5°. Pour into ice-cold brine (800 cc) and extract with ether. Wash and dry the ether layer and concentrate, deeping the temperature below +15°. Add calcium carbonate (3.0 g) and dimethylformamide (70 cc) and distil off residual ether. Reflux one hour, cool and filter; wash the cake with ether. Pour the filtrate into brine and extract with ether. Recrystallize from ethyl acetate-hexane to obtain dl-13-ethyl-17β-acetoxygona-4,6-dien-3-one (0.475 g), m.p. 163°- 177°, λmax. KBr 5.77, 6.0 μ; λmax. EtOH 283 mμ (ε24,370).
Workup
- temperatureChill to 0°
- extractionextract with ether
- washWash
- dry with materialdry the ether layer
- concentrationconcentrate
- customthe temperature below +15°
- customAdd calcium carbonate (3.0 g) and dimethylformamide (70 cc) and distil off residual ether
- temperatureReflux one hour
- temperaturecool
- filtrationfilter
- washwash the cake with ether
- additionPour the filtrate into brine
- extractionextract with ether
- customRecrystallize from ethyl acetate-hexane
Sources & evidence
- ORD record
- ord-15b0778d82884458a93921257cbd96eb
- Source dataset
- uspto-grants-1977_01
- Patent number
- US04002746
Reaction notes
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