Ethanol → HCID 21446176, compound

HRID 597736Notes

Reaction equation

HRID 597736 reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][C:3]2(C[CH:10]3[CH2:12][CH2:13][CH:7]2[CH2:8][CH2:9]3)[CH2:2]1.[CH2:14](Br)[CH2:15][C:16]1[CH:21]=C[CH:19]=[CH:18][CH:17]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:29](O)[CH3:30]>>[CH2:2]([N:1]1[CH2:6][CH2:5][CH2:4][CH2:19][C:18]21[CH2:17][CH:16]1[CH2:21][CH2:29][CH:30]2[CH2:14][CH2:15]1)[CH2:3][C:7]1[CH:8]=[CH:9][CH:10]=[CH:12][CH:13]=1

Participants

5

Reactant 4

HCID 702EthanolHCID 7666Phenethyl bromideHCID 11430Potassium CarbonateHCID 21446145HCID 21446145, compound

Product 1

HCID 21446176HCID 21446176, compound

Procedure

An amount of 6.0 g (0.030 mole) of spiro[bicyclo[2.2.2]-octane-2,3'-piperidine] is dissolved in 50 ml of ethanol; additions are then made of 6.8 g (0.033 mole) of phenethylbromide and 10 g (ca. 0.07 mole) of anhydrous potassium carbonate, and the whole subsequently refluxed, with stirring, for 18 hours. The reaction mixture is filtered, and the brown filtrate concentrated in vacuo (ca. 12 Torr). The viscous residue is distributed between 100 ml of methylene chloride and 100 ml of water. The methylene chloride phase is separated, and the aqueous phase afterwards washed twice with 100 ml of methylene chloride. The combined methylene chloride solutions are dried over sodium sulphate, and then concentrated in vacuo (ca. 12 Torr). There is obtained viscous 1'-phenethylspiro[bicyclo[2.2.2]octane-2,2'-piperidine]. This is dissolved in 50 ml of ether and there is then added to the solution, with stirring, 10 ml of saturated ethereal hydrogen chloride solution. The precipitated hydrochloride is filtered off. There is obtained, after recrystallisation from acetone, 1'-phenethyl-spiro[bicyclo[2.2.2]octane2,3'-piperidine]-hydrochloride, M.P. 263° (with decomposition).

Workup

  1. temperaturethe whole subsequently refluxed
  2. filtrationThe reaction mixture is filtered
  3. concentrationthe brown filtrate concentrated in vacuo (ca. 12 Torr)
  4. customThe methylene chloride phase is separated
  5. washthe aqueous phase afterwards washed twice with 100 ml of methylene chloride
  6. dry with materialThe combined methylene chloride solutions are dried over sodium sulphate
  7. concentrationconcentrated in vacuo (ca. 12 Torr)

Sources & evidence

ORD record
ord-576a25222322415d8bdb4b2870adcab3
Source dataset
uspto-grants-1977_03
Patent number
US04015007

Reaction notes

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