HCID 86733484, compound → HCID 53959839, compound
Reaction equation
[CH2:1]([C@:3]12[CH2:11][CH2:10][C:9]3[C:12]4[CH:13]=[CH:14][C:15]([O:20][CH3:21])=[CH:16][C:17]=4[CH2:18][CH2:19][C:8]=3[C:7]1=[CH:6][CH2:5][C:4]12[O:25][CH2:24][CH2:23][O:22]1)[CH3:2].[H][H]>C1C=CC=CC=1.[Pd]>[CH2:1]([C@:3]12[CH2:11][CH2:10][C:9]3[C:12]4[CH:13]=[CH:14][C:15]([O:20][CH3:21])=[CH:16][C:17]=4[CH2:18][CH2:19][C:8]=3[C@@H:7]1[CH2:6][CH2:5][C:4]12[O:22][CH2:23][CH2:24][O:25]1)[CH3:2]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Hydrogenate 13β -ethyl-3-methoxy-17,17-ethylenedioxygona-1,3,5(10),8,14-pentaene (2.0 g.) in benzene (70 cc.) at atmospheric pressure using a 5% palladium on calcium carbonate catalyst (0.70 g.). Uptake of hydrogen ceases after 150 cc. has been absorbed. Isolate the product and recrystallize from 95% ethanol to obtain the title product (1.3 g.), m.p. 135°-137°; ultraviolet absorption peak at 2.78 mμ (15,100).
Workup
- customhas been absorbed
- customIsolate the product
- customrecrystallize from 95% ethanol
Sources & evidence
- ORD record
- ord-1eb0af7d44424be0aeaf9460dfa598c7
- Source dataset
- uspto-grants-1977_01
- Patent number
- US04002746
Reaction notes
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