Acetic Acid → HCID 86749096, compound

HRID 2294073Notes

Reaction equation

HRID 2294073 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]=1

Participants

6

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

  1. filtrationFiltered
  2. customevaporated filtrate

Sources & evidence

ORD record
ord-5f0189ebd8de4f1680ee90b36156bc7b
Source dataset
uspto-grants-1997_11
Patent number
US05688805

Reaction notes

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