Cyclobutanecarbonyl chloride → HCID 12804761, compound

HRID 1733322Notes

Reaction equation

HRID 1733322 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][C:5]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)([OH:8])[CH2:4][CH2:3]1.[CH:22]1([C:26]([Cl:28])=[O:27])[CH2:25][CH2:24][CH2:23]1>CCOCC>[ClH:28].[CH:22]1([C:26]([O:8][C:5]2([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[CH2:4][CH2:3][N:2]([CH3:1])[CH2:7][CH2:6]2)=[O:27])[CH2:25][CH2:24][CH2:23]1

Participants

4

Reactant 2

HCID 78705Cyclobutanecarbonyl chlorideHCID 12542600HCID 12542600, compound

Product 1

HCID 12804761HCID 12804761, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

2.0 g of 1-methyl-4-(α-phenyl-2-tolyl)-4-piperidinol, Example 1, is treated with 10 g of cyclobutanecarbonyl chloride with stirring and cooling. The reaction mixture is stirred for 48 hours at ambient temperature, diluted with 15 ml of ether and then stirred for 2 hours. The resulting precipitate is collected by suction filtration, the filter cake washed well with ether and dried in vacuo over sodium hydroxide pellets. The filter cake is recrystallized twice from an acetone-ether mixture to give colorless crystals, mp 194.5°-195° C. of 4-cyclobutylcarbonyloxy-1-methyl-4-(α-phenyl-2-tolyl)piperidine hydrochloride.

Workup

  1. temperaturecooling
  2. stirringThe reaction mixture is stirred for 48 hours at ambient temperature
  3. stirringstirred for 2 hours
  4. filtrationThe resulting precipitate is collected by suction filtration
  5. washthe filter cake washed well with ether
  6. dry with materialdried in vacuo over sodium hydroxide pellets
  7. customThe filter cake is recrystallized twice from an acetone-ether mixture

Sources & evidence

ORD record
ord-5e4cbf4619fe4e4abd4b06e3e7743302
Source dataset
uspto-grants-1980_12
Patent number
US04241071

Reaction notes

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