Benzyl chloroformate → Benzyl 4-(2-hydroxyethyl)piperidine-1-carboxylate

HRID 374810Notes

Reaction equation

HRID 374810 reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([CH2:7][CH2:8][OH:9])[CH2:3][CH2:2]1.C(=O)([O-])O.[Na+].[CH2:15]([O:22][C:23](Cl)=[O:24])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>O>[CH2:15]([O:22][C:23]([N:1]1[CH2:6][CH2:5][CH:4]([CH2:7][CH2:8][OH:9])[CH2:3][CH2:2]1)=[O:24])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

Participants

5

Reactant 3

HCID 10387Benzyl chloroformateHCID 739534-PiperidineethanolHCID 516892Sodium Bicarbonate

Product 1

HCID 13971210Benzyl 4-(2-hydroxyethyl)piperidine-1-carboxylateYield 65%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

50 g of 4-piperidine ethanol and 49.2 g of sodium hydrogencarbonate were dissolved in 480 ml of water, in which 55.2 ml of benzyloxycarbonyl chloride was gradually dropped under ice-cooling conditions, followed by agitation for 1 hour as it is. The reaction solution was extracted with chloroform and dried with anhydrous magnesium sulfate. The sulfate was filtered off and the solvent was distilled off, after which the resultant residue was subjected to silica gel column chromatography (developing solvent; ethyl acetate:hexane=30:70) to obtain 66.0 g of the captioned compound (yield: 65%).

Workup

  1. additionwas gradually dropped under ice-
  2. temperaturecooling conditions
  3. extractionThe reaction solution was extracted with chloroform
  4. dry with materialdried with anhydrous magnesium sulfate
  5. filtrationThe sulfate was filtered off
  6. distillationthe solvent was distilled off

Sources & evidence

ORD record
ord-d6e4a26dd71544caa1b68eaee738e51b
Source dataset
uspto-grants-1996_01
Patent number
US05482937

Reaction notes

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