Cyclopentanone → HCID 20316885, compound
Reaction equation
[C:1]1(=O)[CH2:5][CH2:4][CH2:3][CH2:2]1.Br.[NH2:8][CH:9]1[CH2:18][CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[C:14]([OH:20])[C:15]=2[OH:19])[C:10]1=[O:21]>C(O)C>[C:1]1(=[N:8][CH:9]2[CH2:18][CH2:17][C:16]3[C:11](=[CH:12][CH:13]=[C:14]([OH:20])[C:15]=3[OH:19])[C:10]2=[O:21])[CH2:5][CH2:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a mixture of 20 volume parts of cyclopentanone and 100 volume parts of ethanol is dissolved 1 part of 2-amino-5,6-dihydroxy-3,4-dihydro-1(2H)-naphthalenone hydrobromide to produce 2-cyclopentylideneamino-5,6-dihydroxy-3,4-dihydro-1(2H)-naphthalenone. The resulting mixture is subjected to catalytic reduction with 0.1 part of platinum dioxide and 0.39 part of anhydrous sodium acetate at ordinary temperature and pressure.
Sources & evidence
- ORD record
- ord-2f3969b69d8d49d385af1393c5c8e9a5
- Source dataset
- uspto-grants-1978_08
- Patent number
- US04104402
Reaction notes
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