Acetic Acid → HCID 86749096, compound
Reaction equation
[CH:1]1[C:11]2[CH2:10][CH2:9][C:8]3[CH:12]=[CH:13][CH:14]=[CH:15][C:7]=3[CH:6]([C:16]3[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.[H][H].CCOCC.[C:29]([OH:32])(=[O:31])[CH3:30]>[Pt]=O>[CH:12]1[C:8]2[CH2:9][CH2:10][C:11]3[CH:1]=[CH:2][CH:3]=[CH:4][C:5]=3[CH:6]([CH:16]3[CH2:21][CH2:20][CH2:19][N:18]([CH2:30][C:29]([OH:32])=[O:31])[CH2:17]3)[C:7]=2[CH:15]=[CH:14][CH:13]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Dissolved 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-pyridine (0.95 g, 3.5 mmol) in 50 mL of glacial acetic acid. Added platinum oxide catalyst (0.2 g), and shook on Paar shaker at 59 psi of hydrogen pressure for 24 hours. Filtered, and evaporated filtrate. Crystallized product from ether to give 1.14 g (100% yield) of 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-piperidine acetic acid as a white solid.
Workup
- filtrationFiltered
- customevaporated filtrate
Sources & evidence
- ORD record
- ord-5f0189ebd8de4f1680ee90b36156bc7b
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05688805
Reaction notes
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