1-Bromo-3-chloropropane → Piperidine, 1-(3-chloropropyl)-

HRID 502741Notes

Reaction equation

HRID 502741 reaction equation
Br[CH2:2][CH2:3][CH2:4][Cl:5].[NH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1>C1COCC1>[Cl:5][CH2:4][CH2:3][CH2:2][N:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1

Participants

4

Procedure

A mixture of 1-bromo-3-chloropropane (65.6 g, 0.417 mol) and piperidine (62 ml, 0.625 mol) in anhydrous THF (200 ml) was heated to reflux for 24 h. The mixture was cooled to RT and filtered to remove solids. The organics were concentrated under in vacuo. The resultant residue was taken up in 2N HCl and washed twice with ethyl acetate. The aqueous layer was basicified with 2N NaOH to pH 14. The compound was extracted three times with ethyl acetate and the combined organics dried over anhydrous magnesium sulfate. The solution was then concentrated under reduced pressure to give the desired compound as a yellowish oil.

Workup

  1. temperaturewas heated
  2. temperatureto reflux for 24 h
  3. filtrationfiltered
  4. customto remove solids
  5. concentrationThe organics were concentrated under in vacuo
  6. washwashed twice with ethyl acetate
  7. extractionThe compound was extracted three times with ethyl acetate
  8. dry with materialthe combined organics dried over anhydrous magnesium sulfate
  9. concentrationThe solution was then concentrated under reduced pressure

Sources & evidence

ORD record
ord-388f75754b3e4bc8bbf82aa5eaf66468
Source dataset
uspto-grants-2010_08
Patent number
US07776869B2

Reaction notes

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